Method of treating diseases and conditions associated with an altered level of amyloid beta peptides and new enolcarboxamide compounds

ABSTRACT

A method of treating or preventing of a disease or condition associated with an increased level of isoforms of amyloid β peptides (Aβ) and/or with a changed ratio of levels of Aβ isoforms and/or with the formation of plaques containing amyloid β peptide (Aβ) isoforms in a mammal comprising administering to said mammal an therapeutically effective amount of a compound selected from the formulas Ia, Ib  
                 
 
wherein V, W, Y, R 2 , R 3 , R 5 , R 6 , L1 and i are defined as in claim 1.

The invention relates to a method of treating or preventing of a diseaseor condition associated with an increased level of one or more isoformsof amyloid β peptides (Aβ) and/or with a changed ratio of levels of Aβisoforms and/or with the formation of plaques containing one or moreamyloid β peptide (Aβ) isoforms in a mammal. Furthermore this inventionrelates to the use of at least one compound selected from the formula Iaand Ib as defined herein for the manufacture of a medicament forpreventing or treating of a disease or condition associated with anincreased level of one or more isoforms of amyloid β peptides (Aβ)and/or with a changed ratio of levels of Aβ isoforms and/or with theformation of plaques containing one or more amyloid β peptide (Aβ)isoforms in a mammal. In addition, this invention is related to apharmaceutical composition comprising at least one compound selectedfrom the formula Ia and Ib as defined herein and at least onepharmaceutically acceptable carrier or diluent. Furthermore the presentinvention is related to the use of said compounds for modulating theactivity of γ-secretase. In addition the present invention is related tothe use of said compounds for the manufacture of a medicament formodulating the activity of γ-secretase. The present invention is alsorelated to the new compounds selected from the group of formulas I.3a,I.3b, I.4a, I.4b, IIa, IIb, I.2.2a, I.2.2b, I.5.1a, I.5.1b, I.6.1a, andI.6.1b, which are active in lowering levels of amyloid β peptides.

Alzheimer's disease (AD) is a progressive degenerative disease of thebrain primarily associated with aging. There also exists a hereditaryform called familial Alzheimer's disease (FAD). The non-hereditary formof Alzheimer which is associated with aging is also called sporadicAlzheimer. In the following the term Alzheimers's disease or AD alsoencompasses said hereditary form. Clinical presentation of AD ischaracterized by loss of memory, cognition, reasoning, judgement, andorientation. As the disease progresses, motor, sensory, and linguisticabilities are also affected until there is global impairment of multiplecognitive functions. These cognitive losses occur gradually, buttypically lead to severe impairment and death in the range of four totwelve years.

Alzheimer's disease is characterized by two major pathologicobservations in the brain: neurofibrillary tangles (NFT) and betaamyloid (or neuritic) plaques, comprised predominantly of an aggregateof a peptide fragment known as amyloid β, A beta or Aβ. Individuals withAD exhibit characteristic beta-amyloid deposits in the brain (betaamyloid plaques) and in cerebral blood vessels (beta amyloid angiopathy)as well as neurofibrillary tangles. Neurofibrillary tangles occur notonly in Alzheimer's disease but also in other dementia-inducingdisorders. On autopsy, large numbers of these lesions are generallyfound in areas of the human brain important for memory and cognition.

Smaller numbers of these lesions in a more restricted anatomicaldistribution are found in the brains of most aged humans who do not haveclinical AD.

Amyloidogenic plaques and vascular amyloid angiopathy also characterizethe brains of individuals with Trisomy 21 (Down's Syndrome), HereditaryCerebral Hemorrhage with Amyloidosis of the Dutch-Type (HCHWA-D), andother neurodegenerative disorders. Beta-amyloid is a neurotoxic peptidethat exists in several isoforms, now believed to be a causativeprecursor or factor in the development of disease. Deposition of A betain areas of the brain responsible for cognitive activities is a majorfactor in the development of AD. Beta-amyloid plaques are predominantlycomposed of amyloid beta peptide (A beta, also sometimes designatedbetaA4). A beta peptide is derived by sequential proteolysis of theamyloid precursor protein (APP) and is comprised of about 34 to 42 aminoacids. Several proteases called secretases are involved in theprocessing of APP. Aβ consists predominantly of two forms, Aβ₄₀ andAβ₄₂. Although Aβ₄₀ is the predominant form, evidence suggests that Aβ₄₂is the pathogenic form. In addition to Aβ₄₀, and Aβ₄₂, the processing ofAPP generates other Aβ forms such as Aβ₃₉, Aβ₃₈, Aβ₃₇, and Aβ₃₄.

Cleavage of APP at the N-terminus of the A beta peptide bybeta-secretase (BACE) and at the C-terminus by one or moregamma-secretases constitutes the beta-amyloidogenic pathway, i.e., thepathway by which A beta is formed. Cleavage of APP by alpha-secretaseproduces alpha-sAPP, a secreted form of APP that does not result inbeta-amyloid plaque formation. This alternate pathway precludes theformation of A beta peptide.

An aspartyl protease has been identified as the enzyme responsible forprocessing of APP at the beta-secretase cleavage site. Thebeta-secretase enzyme has been disclosed using varied nomenclature,including BACE, Asp2, and Memapsin2.

Gamma-secretase is a multiprotein complex that consists of at least fourmembrane-bound proteins: presenilin (PS), nicastrin, APH-1, and PEN-2.All of these components are required for proper maturation and activityof the complex while the enzymatic core of this activity may residewithin presenilin itself. The gamma-secretase activity displays aflexibel sequence specificity. Therefore, A beta peptides of varyinglengths, such as Aβ₃₈, Aβ₄₀, Aβ₄₂ are generated.

It has been found that mutations in PS1 and PS2 which cause familialAlzheimer's disease (FAD) also alter APP processing and causeoverproduction of Aβ₄₂ peptides such that the ratio of levels of Aβ₄₀ toAβ₄₂ is changed (See also literature cited by Sisodia S S andGeorge-Hyslop P H, 2002. γ Secretase, notch, Aβ and Alzheimer's Disease:where do the presenilins fit in? Nature Reviews Neuroscience, 3,281-290).

Several lines of evidence indicate that progressive cerebral depositionof beta-amyloid peptide (A beta) plays a seminal role in thepathogenesis of AD and can precede cognitive symptoms by years ordecades. See, for example, Selkoe, 1991, Neuron 6: 487-498. Release of Abeta from neuronal cells grown in culture and the presence of A beta incerebrospinal fluid (CSF) of both normal individuals and AD patients hasbeen demonstrated. See, for example, Seubert et al., 1992, Nature 359:325-327.

Various pharmaceutical agents have been proposed for the treatment ofAlzheimer's disease but without any real success.

In the WO 98/20864, the use of non-steroidal antiinflammatory compoundsfor the prevention and the treatment of glutamate receptor-mediatedneuronal damages is described. Among many other compounds piroxicam,tenoxicam and meloxicam are mentioned as NSAIDs. The disease Alzheimeris listed as belonging to the group of glutamate receptor-mediatedneuronal damages.

In the EP 0 642 336 A, the use of non-steroidal antiinflammatorysubstances which have the ability to inhibit prostaglandin synthesis inthe human being is described for the treament of dementia.

In the WO 01/78721, a method of preventing, delaying or reversing theprogression of Alzheimer's disease by the administration of Aβ₄₂lowering agents is described. Suitable Aβ₄₂ lowering agents aremeclofenamic acid, flufenamic acid, fenoprofen, flurbiprofen, carprofen,indomethacin, sulindac sulfide, ibuprofen, ketoprofen, etc. which belongto the group of nonsteroidal antiinflammatory drugs (NSAIDs). On theother hand not all NSAIDs show a Aβ₄₂ lowering activity. According tothe table 3 as depicted in the WO 01/78721 meloxicam, piroxicam andisoxicam, which all belong to the class of the enol carboxamides, do notlower or even increase the Aβ₄₂ level.

Evidence has been provided that specific compounds which belong to theclass of NSAIDs may interact with gamma-secretase, either directly orindirectly:

-   -   Eriksen J L et al., 2003. NSAIDs and enantiomers of flurbiprofen        target γ-secretase and lower Aβ₄₂ in vivo., J. Clin. Invest.        112, 3, 440-449;    -   Weggen S et al., 2003. Evidence that nonsteroidal        anti-inflammatory drugs decrease amyloid β₄₂ production by        direct modulation of γ-secretase activity. J. Biol. Chem. 278        (34), 31831-31837;    -   Takahashi Y et al., 2003. Sulindac Sulfide is a noncompetitive        γ-secretase inhibitor that preferentially reduces Aβ₄₂        generation, J. Biol. Chem. 278 (20), 18664-18670;    -   Weggen S et al., 2001. A subset of NSAIDs lower amyloidogenic        Aβ₄₂ independently of cyclooxygenase activity. Nature 414,        212-216;    -   Zhou Y et al., 2003. Nonsteroidal anti-inflammatory drugs can        lower amyloidogenic Aβ₄₂ by inhibiting Rho, Science, 302,        1215-1217.

At present there are no non symptomatic effective treatments forhalting, preventing, or reversing the progression of Alzheimer'sdisease. Therefore, there is an urgent need for pharmaceutical agentswith sufficient plasma and/or brain stability capable of slowing theprogression of Alzheimer's disease and/or preventing it in the firstplace.

SUMMARY OF THE INVENTION

Surprisingly, it has been found that compounds selected from the formulaIa and Ib as defined in the following have an activity to reduce orinhibit the formation of isoforms of amyloid β peptides (Aβ), to changethe ratio of levels of isoforms of Aβ and/or to modulate the activity ofγ-secretase.

Therefore, the present invention relates to a method of treating orpreventing of a disease or condition associated with an increased levelof one or more isoforms of amyloid β peptides (Aβ) and/or with a changedratio of levels of Aβ isoforms and/or with the formation of plaquescontaining one or more amyloid β peptide (Aβ) isoforms in a mammalcomprising administering to said mammal a therapeutically effectiveamount of at least one compound selected from the formulas Ia, Ib

wherein

-   - - - - represents a single or a double bond, such that the ring    containing the groups V and W is a phenyl, a furanyl or a thiophenyl    ring;-   V is defined as —CR¹═ or Q, and-   in case W is Q, then V is a single bond;-   W is defined as ═CR⁴— or Q, and-   in case V is Q, then W is a single bond;-   Q is O or S;-   Y is —(C═O)— or —(SO₂)—;-   R¹, R⁴ are each independently selected from the group consisting of    H, F, Cl, Br, CN, CF₃, C₁₋₄-alkyl and C₁₋₄-alkoxy; and-   R², R³ are each independently selected from the group consisting of    H, F, Cl, Br, CN, CF₃, C₁₋₄-alkyl and C₁₋₄-alkoxy; or-   in case V is —CR¹═ and W is ═CR⁴—, the substituents R² and R³ may be    linked together forming with the C-atoms to which they are attached    to a C₅₋₇-cycloalkyl, C₅₋₇-cycloalkenyl or a phenyl group, wherein    the cycloalkyl, cycloalkenyl or phenyl ring may be substituted with    one or more substituents L2; or-   in case V is —CR¹═ and W is ═CR⁴—, the substituents R¹ and R² may be    linked together forming with the C-atoms to which they are attached    to a C₅₋₇-cycloalkyl, C₅₋₇-cycloalkenyl or a phenyl group, wherein    the cycloalkyl, cycloalkenyl or phenyl ring may be substituted with    one or more substituents L2;-   R⁵ is selected from the group consisting of H, C₁₋₄-alkyl,    C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₃-alkyl, phenyl and    phenyl-C₁₋₃-alkyl, wherein a cycloalkyl or phenyl ring may be    substituted with one or more substituents independently selected    from the group consisting of F, Cl, Br, CN, CF₃, C₁₋₄-alkyl,    C₁₋₄-alkoxy, C₁₋₄-alkylcarbonyl;-   R⁶ is H or C₁₋₄-alkyl;-   L1 is each independently selected from the group consisting of    C₁₋₄-alkyl, C₁₋₃-alkoxy, F, Cl, Br, CN, NO₂ and CF₃;-   L2 is each independently selected from the group consisting of    C₁₋₄-alkyl, F, Cl, Br, CN and CF₃;-   i is 0, 1, 2, 3, 4 or 5;    or a pharmaceutically acceptable salt thereof.

Compounds which can be described by a general formula Ia or Ib weretested in view of their COX-2/COX-1 selectivity in comparison with thenonsteroidal antiinflammatory drug meloxicam (E. S. Lazer et al., J.Med. Chem. 1997, 40, 980-989). Furthermore thienothiazine derivativesare described in the U.S. Pat. No. 4,175,085, U.S. Pat. No. 4,187,303and U.S. Pat. No. 4,090,020 as being useful as anti-inflammatroy,analgesic and anti-rheumatic agents. In addition3,4-dihydro-2H-1,2-benzothiazine 1,1-dioxide derivatives and their useas anti-inflammatory agents are described in the U.S. Pat. No.3,591,584.

As the compounds according to this invention belong to the NSAID groupof enol carboxamides and show a structural similarity with meloxicam, itis completely surprising that these compounds exhibit a loweringactivity on Aβ isoforms and/or modulate the activity of γ-secretase.Analysing the results as disclosed in the WO 01/78721 with regard toenol carboxamides and especially with regard to meloxicam, the personskilled in the art would not have expected to identify other members ofthe group of the enol carboxamides as effective agents to lower thelevel of Aβ isoforms.

Therefore, the compounds, compositions, and methods of the presentinvention are effective to inhibit the production of amyloid β peptides(Aβ) and to treat or prevent human or veterinary diseases or conditionsassociated with a pathological form of amyloid β peptides (Aβ), inparticular of Aβ₄₂.

The compounds, compositions, and methods of the invention are useful fortreating humans who have Alzheimer's Disease (AD), for helping preventor delay the onset of AD, for treating patients with mild cognitiveimpairment (MCI), and preventing or delaying the onset of AD in thosepatients who would otherwise be expected to progress from MCI to AD, fortreating Down's syndrome, for treating Hereditary Cerebral Hemorrhagewith Amyloidosis of the Dutch Type, for treating cerebral beta-amyloidangiopathy and preventing its potential consequences such as single andrecurrent lobar hemorrhages, for treating other degenerative dementias,including dementias of mixed vascular and degenerative origin, fortreating dementia associated with Parkinson's disease, dementiaassociated with progressive supranuclear palsy, dementia associated withcortical basal degeneration, and diffuse Lewy body type AD.

According to another embodiment those compounds and compositions used ina method according to this invention are preferred which exhibit a COXinhibiting activity, especially a COX-2 inhibiting activity, inparticular those which inhibit COX-2 selectively. Such compounds andcompositions are expected to be particularly useful for treating and/orpreventing those inflammatory diseases or inflammatory conditionsassociated with an increased level of one or more isoforms of amyloid βpeptides (Aβ) and/or with a changed ratio of levels of Aβ isoformsand/or with the formation of plaques containing one or more amyloid βpeptide (Aβ) isoforms in a mammal. Furthermore such compounds andcompositions are expected to be particularly useful for a combinedtreatment and/or prevention of an inflammatory disease or inflammatorycondition and a disease or condition associated with an increased levelof one or more isoforms of amyloid β peptides (Aβ) and/or with a changedratio of levels of Aβ isoforms and/or with the formation of plaquescontaining one or more amyloid β peptide (Aβ) isoforms. For example,such compounds and compositions are expected to be useful for treatinghumans who are diagnosed to have for example both Alzheimer's disease(AD) and a disease associated with inflammatory conditions, inparticular Parkinson's disease.

Therefore, in another aspect the present invention describes the use ofat least one compound selected from the formula Ia and Ib as definedhereinbefore and hereinafter, or a pharmaceutically acceptable saltthereof, for the manufacture of a medicament for preventing or treatingof one or more diseases or conditions associated with an increased levelof one or more amyloid β peptides (Aβ) and/or with a changed ratio oflevels of Aβ isoforms and/or with the formation of plaques containingone or more amyloid β peptides (Aβ) in a mammal.

In a further aspect the present invention relates to the use of at leastone compound selected from the formulas Ia, Ib as defined hereinbeforeand hereinafter, or a pharmaceutically acceptable salt thereof, formodulating the activity of γ-secretase.

Therefore the present invention also relates to the use of at least onecompound selected from the formulas Ia, Ib as defined hereinbefore andhereinafter, or a pharmaceutically acceptable salt thereof, for themanufacture of a medicament for modulating the activity of γ-secretase.

In addition the present invention relates to a pharmaceuticalcomposition comprising at least one compound selected from the formulaIa and Ib as defined hereinbefore and hereinafter, or a pharmaceuticallyacceptable salt thereof, and at least one pharmaceutically acceptablecarrier or diluent.

The inhibitory activities of the compounds of the formula Ia and Ib ofthe present invention are readily demonstrated, for example, using oneor more of the assays described herein or known in the art.

A further aspect of the present invention is related to new compoundsselected from the group of formulas I.3a, I.3b, I.4a, I.4b

-   Y is —(C═O)— or —(SO₂)—;-   R¹, R³, R⁴ are each independently selected from the group consisting    of H, F, Cl, Br, CN, CF₃, C₁₋₄-alkyl and C₁₋₄-alkoxy;-   R⁵ is selected from the group consisting of H, C₁₋₄-alkyl,    C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₃-alkyl, phenyl and    phenyl-C₁₋₃-alkyl, wherein the phenyl ring of the phenyl or the    phenyl-alkyl group may be substituted with one or more substituents    independently selected from the group consisting of F, Cl, Br, CN,    CF₃, C₁₋₄-alkyl, C₁₋₄-alkylcarbonyl;-   R⁶ is H or C₁₋₄-alkyl;-   L1 is each independently selected from the group consisting of    C₁₋₄-alkyl, C₁₋₃-alkoxy, F, Cl, Br, CN, NO₂ and CF₃;-   L2 is each independently selected from the group consisting of    C₁₋₄-alkyl, F, Cl, Br, CN and CF₃;-   i is 0, 1, 2, 3, 4 or 5;-   j is 0, 1, 2 or 3;-   m is 0, 1 or 2;    or a pharmaceutically acceptable salt thereof.

Another further aspect of the present invention is a compound selectedfrom the formulas IIa, IIb

wherein

-   - - - - represents a single or a double bond, such that the ring    containing the groups V and W is a phenyl, a furanyl or a thiophenyl    ring;-   V is defined as —CR¹═ or Q, and-   in case W is Q, then V is a single bond;-   W is defined as ═CR⁴— or Q, and-   in case V is Q, then W is a single bond;-   Q is O or S;-   Y is —(C═O)— or —(SO₂)—;-   R¹, R⁴ are each independently selected from the group consisting of    H, F, Cl, Br, CN, CF₃, C₁₋₄-alkyl and C₁₋₄-alkoxy; and-   R², R³ are each independently selected from the group consisting of    H, F, Cl, Br, CN, CF₃, C₁₋₄-alkyl and C₁₋₄-alkoxy; or-   in case V is —CR¹═ and W is ═CR⁴—, the substituents R² and R³ may be    linked together forming with the C-atoms to which they are attached    to a C₅₋₇-cycloalkyl, C₅₋₇-cycloalkenyl or a phenyl group, wherein a    cycloalkyl, cycloalkenyl or phenyl ring may be substituted with one    or more substituents L2; or-   in case V is —CR¹═ and W is ═CR⁴—, the substituents R¹ and R² may be    linked together forming with the C-atoms to which they are attached    to a C₅₋₇-cycloalkyl, C₅₋₇-cycloalkenyl or a phenyl group, wherein a    cycloalkyl, cycloalkenyl or phenyl ring may be substituted with one    or more substituents L2;-   R⁶ is H or C₁₋₄-alkyl;-   L1 is each independently selected from the group consisting of    C₁₋₄-alkyl, C₁₋₃-alkoxy, F, Cl, Br, CN, NO₂ and CF₃;-   L2, L3 is each independently selected from the group consisting of    C₁₋₄-alkyl, F, Cl, Br, CN and CF₃;-   i is 0, 1, 2, 3, 4 or 5;-   k is 1, 2, 3, 4 or 5;    or a pharmaceutically acceptable salt thereof.

Another further aspect of the present invention is a compound selectedfrom the formulas I.2.2a, I.2.2b

wherein

-   R⁵ is selected from the group consisting of H, C₁₋₄-alkyl,    C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₃-alkyl, phenyl and    phenyl-C₁₋₃-alkyl, wherein the phenyl ring of the phenyl or the    phenyl-alkyl group may be substituted with one or more substituents    independently selected from the group consisting of F, Cl, Br, CN,    CF₃, C₁₋₄-alkyl, C₁₋₄-alkoxy, C₁₋₄-alkylcarbonyl;-   R⁶ is H or C₁₋₄-alkyl;-   L1 is each independently selected from the group consisting of    C₁₋₄-alkyl, C₁₋₃-alkoxy, F, Cl, Br, CN, NO₂ and CF₃, with the    proviso that L1 is not Cl in para-position if index i is 1 and R⁵ is    methyl;-   i is 0, 1, 2, 3, 4 or 5;    or a pharmaceutically acceptable salt thereof.

Another further aspect of the present invention is a compound selectedfrom the formulas I.5.1a, I.5.1b, I.6.1a and I.6.1b

wherein

-   Q is O or S;-   R², R³ are independently selected from the group consisting of F,    Br, CN, CF₃, C₁₋₄-alkyl and C₁₋₄-alkoxy;-   R⁵ is selected from the group consisting of H, C₁₋₄-alkyl,    C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₃-alkyl, phenyl and    phenyl-C₁₋₃-alkyl, wherein the phenyl ring of the phenyl or the    phenyl-alkyl group may be substituted with one or more substituents    independently selected from the group consisting of F, Cl, Br, CN,    CF₃, C₁₋₄-alkyl, C₁₋₄-alkoxy, C₁₋₄-alkylcarbonyl;-   R⁶ is H or C₁₋₄-alkyl;-   L1 is each independently selected from the group consisting of    C₁₋₄-alkyl, C₁₋₃-alkoxy, F, Cl, Br, CN, NO₂ and CF₃, with the    proviso that L1 is not Cl in para-position if index i is 1 and R⁵ is    methyl;-   i is 0, 1, 2, 3, 4 or 5;    or a pharmaceutically acceptable salt thereof.

These new compounds of the formulas I.3a, I.3b, I.4a, I.4b, IIa, IIb,I.2.2a, I.2.2b, I.5.1a, I.5.1b, I.6.1a, and I.6.1b belong to the groupof compounds as described by the formulas Ia and Ib and thus alsopossess valuable Aβ lowering activity, in particular Aβ₄₂ loweringactivity, a γ-secretase modulating activity and/or an activity to changethe ratio of levels of isoforms of Aβ.

DETAILED DESCRIPTION OF THE INVENTION

The term “compound of the invention” refers to a compound selected fromthe formula Ia and Ib as defined hereinbefore and hereinafter.

The term “mammal” refers to rats, mice, guinea pigs, hares, dogs, cats,sheep, horses, pigs, cattle, cows, monkeys and also humans. Inparticular the term “mammal” refers to humans.

The terms “level of Aβ,” “level of isoforms of Aβ,” “Aβ level,” etc.,refer to a level of the specified Aβ isoform as determined for examplein plasma fluid, brain fluid, cerebrospinal fluid (CSF) or in neurons orglia. Suitable methods for the determination of levels of Aβ are knownby the person skilled in the art and are described in the scientificliterature. For example suitable methods are ELISA and massspectrometry.

The terms “increased level of Aβ,” “increased level of isoforms of Aβ,”etc., refer to those levels of isoforms of Aβ as described above whichare elevated in an individual diagnosed having or developing a diseaseor conditions according to this invention, in particular with diagnosedAlzheimer's disease, compared to individuals diagnosed not having ordeveloping such a disease or condition.

In the following the groups and substituents V, W, Q, Y, R¹, R², R³, R⁴,R⁵, R⁶, L1, L2, L3, and the indizes i, j, and k are defined ashereinbefore and hereinafter.

Substituents and groups which appear twice or more in a formula may havethe same or different meanings as defined.

According to a first embodiment of the present invention the compoundadministered is chosen from the formulas I.1a, I.1b, preferably from theformula I.1a,

wherein the group Y, the substituents R¹, R⁴, R⁵, R⁶ and L1 and theindex i are defined as hereinbefore and hereinafter, and

-   R², R³ are each independently selected from the group consisting of    H, F, Cl, Br, CN, CF₃, C₁₋₄-alkyl and C₁₋₄-alkoxy; or    or a pharmaceutically acceptable salt thereof.

According to a second embodiment of the present invention the compoundadministered is chosen from the formulas I.2a, I.2b, preferably from theformula I.2a,

wherein the group Y, the substituents R¹, R⁴, R⁵, R⁶, L1 and L2 and theindex i are defined as hereinbefore and hereinafter,wherein j is 0, 1, 2, 3 or 4;or a pharmaceutically acceptable salt thereof.

According to a third embodiment of the present invention the compoundadministered is chosen from the formulas I.3a, I.3b, I.4a, I.4b

wherein the group Y, the substituents R¹, R³, R⁴, R⁵, R⁶, L1 and L2 andthe index i are defined as hereinbefore and hereinafter,

-   j is 0, 1, 2 or 3; and-   m is 0, 1 or 2;    or a pharmaceutically acceptable salt thereof.

The index j is preferably 0, 1 or 2, in particular 0 or 1. Mostpreferably the index j is 0.

The index m is preferably 0 or 1, most preferably 1.

In said third embodiment the compounds of the formulas I.3a and I.3b, inparticular of I.3a are preferred.

According to a fourth embodiment of the present invention the compoundadministered is chosen from the formulas I.5a, I.5b, I.6a, I.6b

wherein the groups Q and Y, the substituents R⁵, R⁶ and L1 and the indexi are defined as hereinbefore and hereinafter,

-   R², R³ are each independently selected from the group consisting of    H, F, Cl, Br, CN, CF₃, C₁₋₄-alkyl and C₁₋₄-alkoxy; or    or a pharmaceutically acceptable salt thereof.

In the fourth embodiment the compounds of the formulas I.5a and I.5b, inparticular of I.5a are preferred.

In said fourth embodiment the preferred meaning of the group Q is S.

In the method according to this invention those compounds are preferablyadministered in which the group Y is a sulfonyl group.

In the first embodiment of the present invention the group Y is asulfonyl or a carbonyl group.

In the method according to this invention those compounds are preferablyadministered in which the group R⁵ is selected from the group consistingof H, methyl, ethyl, cyclopropyl, phenyl and phenylmethyl, wherein thephenyl ring in the phenyl group or phenylmethyl group may be substitutedwith one, two or more substituents selected from the group consisting ofF, Cl, Br, CN, CF₃, C₁₋₄-alkyl, C₁₋₄-alkoxy or C₁₋₄-alkyl-carbonyl.

Preferred meanings of the group R⁵ are H, methyl, ethyl, cyclopropyl,phenyl and phenylmethyl, wherein the phenyl ring in the phenyl group orphenylmethyl group is unsubstituted or is substituted with one, two orthree substituents selected from the group consisting of F, Cl, Br, CN,CF₃ and methyl.

In the method according to this invention those compounds are preferablyadministered in which the group R⁶ is H or methyl, most preferably H.

Therefore in the method according to the first embodiment preferredcompounds are selected from the formulas I.1.1a, I.1.1b, in particularof the formula I.1.1a

wherein the substituents R¹, R⁴ and L1 and the index i are defined ashereinbefore and hereinafter,

-   R², R³ are each independently selected from the group consisting of    H, F, Cl, Br, CN, CF₃, C₁₋₄-alkyl and C₁₋₄-alkoxy;    or a pharmaceutically acceptable salt thereof.

In the method according to the second embodiment preferred compounds areselected from the formulas I.2.1a, I.2.1b, in particular of the formulaI.2.1a

wherein the substituents R¹, R⁴, L1 and L2 and the index i are definedas hereinbefore and hereinafter,wherein j is 0, 1, 2, 3 or 4;or a pharmaceutically acceptable salt thereof.

In the method according to the third embodiment preferred compounds areselected from the formulas I.3.1a, I.3.1b, in particular of the formulaI.3.1a

wherein the substituents R¹, R⁴, L1, L2 and the index i are defined ashereinbefore and hereinafter,

-   j is 0, 1, 2 or 3    or a pharmaceutically acceptable salt thereof.

In the method according to this invention those compounds withsubstituents R¹, R², R³ and/or R⁴ are preferably administered in whichsaid prevalent groups R¹, R², R³, R⁴ are selected from the groupconsisting of H, F, Cl and methyl.

Furthermore In the method according to this invention preferred meaningsof the substituents L1 and where applicable also L2 and/or L3 are F, Cl,Br, CN, CF₃.

In the compounds administered according to the present invention theindex i is preferably 0, 1, 2 or 3; most preferably 0, 1 or 2; inparticular 1 or 2.

In the compounds administered according to the present invention theindex j, where applicable, is preferably 0, 1 or 2; most preferably 0 or1; in particular 0.

In the following table examples of compounds according to the formulaIa, Ib are listed: 1

2

3

4

5

6

7

8

9

10

11

12

13

14

15

16

17

18

19

20

21

22

23

24

25

26

27

28

29

30

31

32

33

34

35

36

37

38

39

40

41

42

43

44

45

46

47

48

49

50

51

52

53

54

55

56

57

58

59

60

61

62

63

64

65

66

67

68

69

70

In the above table the compounds (1) to (23), in particular (1) to (18)are preferred.

The method according to the present invention is advantageously suitedto treat or prevent a disease or condition which is associated with anincreased level of a pathogenic isoform of Aβ, in particular of Aβ₄₂, orwith a changed ratio of levels of Aβ isoforms, in particular by achanged ratio of a level of Aβ₄₀ to Aβ₄₂, or with the formation ofplaques containing one or more isoforms of Aβ, in particular fibrillarAβ isoforms, especially of Aβ₄₂.

Diseases or conditions which according to this invention canadvantageously be treated or prevented are selected from the groupconsisting of diseases associated with the formation of diffuse andsenile plaques, amyloidosis associated with the formation of Aβisoforms, brain amyloidosis, vascular amyloidosis, age relatedamyloidosis, and central or peripheral amyloid diseases.

Further diseases or conditions which according to this invention canadvantageously be treated or prevented are selected from the groupconsisting of Alzheimer's disease, Down's syndrome, MCI (“Mild CognitiveImpairment”), Heriditary Cerebral Hemorrhage with Amyloidosis of theDutch-Type, Cerebral Amyloid Angiopathy, Traumatic Brain Injury, Stroke,Dementia, Dementia of Alzheimer type (DAT), age associated memoryimpairment (AAMI), Parkinson's Disease and Parkinson's Syndrome, anddiffuse Lewy body type AD.

The method according to this invention is particularly of advantage inthe treatment or prevention of Alzheimer's disease.

Furthermore the method of this invention is particularly suitable in thetreatment or prevention of patients diagnosed both with Alzheimer'sdisease and a disease associated with inflammatory conditions, inparticular Parkinson's disease, when a compound or composition accordingto this invention is administered which exhibits a COX-2 inhibitingactivity, in particular which inhibits COX-2 selectively.

Accordingly the present invention is also related to the use of at leastone compound selected from the formulas Ia, Ib as defined hereinbeforeand hereinafter for the manufacture of a medicament for treating orpreventing of a disease or condition associated with an increased levelof one or more isoforms of amyloid β peptides (Aβ) and/or with a changedratio of levels of Aβ isoforms and/or with the formation of plaquescontaining one or more amyloid β peptide (Aβ) isoforms in a mammal.

The present invention is also related to new compounds which possessvaluable Aβ lowering activity, in particular Aβ₄₂ lowering activity, aγ-secretase modulating activity and/or an activity to change the ratioof levels of isoforms of Aβ.

According to a first embodiment the new compound is selected from thegroup of formulas I.3a, I.3b, I.4a, I.4b, in particular I.3a and I.4a

wherein the groups and substituents Y, R¹, R³, R⁴, R⁵, R⁶, L1, L2 andthe indices i, j and m are defined as hereinbefore.

A preferred meaning of the group Y is sulfonyl.

Preferred meanings of the groups R¹ and R⁴ or R³ and R⁴ areindependently of each other H, F, Cl and methyl.

The substituent R⁵ is preferably selected from the group consisting ofH, methyl, ethyl, cyclopropyl, phenyl and phenylmethyl, wherein thephenyl ring in the phenyl group or phenylmethyl group is unsubstitutedor substituted with 1, 2 or 3 substituents independently of each otherselected from F, Cl, Br, C₁₋₄-alkyl and C₁₋₄-alkyl-carbonyl.

Most preferably R⁵ is methyl.

A preferred meaning of the substituent R⁶ is H.

Preferred meanings of the substituents L1 and L2 are independently ofeach other F, Cl, Br, CN, CF₃ and methyl, whereby L1 may also be NO₂.Most preferably L1 is selected from the group consisting of F, Cl, Br,CH₃ and NO₂.

The index i is preferably 0, 1, 2 or 3; most preferably 0, 1 or 2; inparticular 1 or 2.

The index j is preferably 0, 1 or 2; most preferably 0 or 1; inparticular j is 0.

The index m is preferably 0 or 1; most preferably 1.

Therefore the compounds of the formulas I.3a and I.3b are preferablydescribed by the formulas I.3.1a, I.3.1b, in particular I.3.1a

wherein the substituents R¹, R⁴, L1 and L2 and the index i and j aredefined as hereinbefore, including their pharmaceutically acceptablesalts.

Examples of preferred compounds of the formulas I.3a, I.3b, I.4a, I.4bare (16)

(18)

(21)

(27)

(28)

(29)

(30)

(31)

(32)

(33)

(34)

(35)

including their pharmaceutically acceptable salts.

According to a second embodiment the new compound is selected from thegroup of formulas IIa, IIb, in particular IIa

wherein the groups V, W, Y, R², R³, R⁶, L1, L3 and the indices i and kare defined as hereinbefore, including their pharmaceutically acceptablesalts.

Preferred compounds according to this embodiment are described by theformulas II.1a, II.1b, in particular II.1a

wherein the groups Y, R¹, R⁴, R², R³, R⁶, L1, L3 and the indices i and kare defined as hereinbefore, including their pharmaceutically acceptablesalts.

A preferred meaning of the group Y is sulfonyl.

A preferred meaning of the substituent R⁶ is H.

Preferred meanings of the groups R¹, R², R³, R⁴ are independently ofeach other selected from the group consisting of H, F, Cl and methyl.

Preferred meanings of the substituents L1 and L3 are independently ofeach other F, Cl, Br, CN, CF₃ and methyl, whereby L1 may also be NO₂.Most preferably L3 is selected from the group consisting of F, Cl andBr. Most preferably L1 is selected from the group consisting of Cl, Br,CH₃ and CF₃.

The index i is preferably 0, 1, 2 or 3; most preferably 0, 1 or 2; inparticular 1 or 2.

The index k is preferably 1, 2 or 3; most preferably 1 or 2.

A preferred example of a compound according to this second embodiment is(15)

(36)

(37)

(38)

According to a third embodiment the new compound is selected from thegroup of formulas I.2.2a, I.2.2b, in particular I.2.2a

wherein the groups R⁵, R⁶, L1 and the index i are defined as forformulas I.2.2a and I.2.2b hereinbefore, including theirpharmaceutically acceptable salts.

The substituent R⁵ is preferably selected from the group consisting ofH, C₁₋₄-alkyl, phenyl and phenyl-C₁₋₃-alkyl, wherein the phenyl ring ofthe phenyl or the phenyl-alkyl group may be substituted with one or moresubstituents independently selected from the group consisting of F, Cl,Br, CN, CF₃, C₁₋₄-alkyl, C₁₋₄-alkoxy, C₁₋₄-alkylcarbonyl.

More preferably R⁵ is C₁₋₄-alkyl, most preferably R⁵ is methyl or ethyl,in particular methyl.

A preferred meaning of R⁶ is H.

Preferred meanings of the substituent L1 are independently of each othermethyl, F, Cl, Br, NO₂ and CF₃, with the proviso that L1 is not Cl inpara-position if index i is 1 and R⁵ is methyl.

The index i is preferably 0, 1, 2 or 3, most preferably 0, 1 or 2, inparticular 1 or 2.

Therefore the compounds of the formulas I.2.2a, I.2.2b are preferablydescribed by the formulas I.2.3a, I.2.3b, I.2.4a, I.2.4b in particularI.2.3a, I.2.4a

wherein the substituent L1 and the index i are defined as for formulasI.2.2a and I.2.2b hereinbefore, including their pharmaceuticallyacceptable salts.

Examples of preferred compounds of the formulas I.2.2a and I.2.2b are 39

40

41

42

43

44

45

46

47

48

49

According to a forth embodiment the new compound is selected from thegroup of formulas I.5.1a, I.5.1b, I.6.1a, I.6.1b, in particular I.5.1a,I.6.1a

wherein the groups Q, R², R³, R⁵, R⁶, L1 and the index i are defined asfor formulas I.5.1a, I.5.1b, I.6.1a, I.6.1b hereinbefore, includingtheir pharmaceutically acceptable salts.

Preferably the meaning of substituent R², R³ is C₁₋₄-alkyl, mostpreferably R², R³ is methyl or ethyl.

The substituent R⁵ is preferably selected from the group consisting ofH, C₁₋₄-alkyl, phenyl and phenyl-C₁₋₃-alkyl, wherein the phenyl ring ofthe phenyl or the phenyl-alkyl group may be substituted with one or moresubstituents independently selected from the group consisting of F, Cl,Br, CN, CF₃, C₁₋₄-alkyl, C₁₋₄-alkoxy, C₁₋₄-alkylcarbonyl.

More preferably R⁵ is C₁₋₄-alkyl, most preferably R⁵ is methyl.

A preferred meaning of R⁶ is H.

Preferred meanings of the substituent L1 are independently of each othermethyl, methoxy, F, Cl, Br, NO₂ and CF₃, with the proviso that L1 is notCl in para-position if index i is 1 and R⁵ is methyl.

The index i is preferably 0, 1, 2 or 3, most preferably 0, 1 or 2, inparticular 1 or 2.

Therefore the compounds of the formulas I.5.1a, I.5.1b, I.6.1a, I.6.1bare preferably described by the formulas I.5.2a, I.5.2b, I.6.2a, I.6.2bin particular I.5.2a, I.6.2a

wherein the groups Q, L1 and the index i are defined as for formulasI.5.1a, I.5.1b, I.6.1a, I.6.1b hereinbefore, including theirpharmaceutically acceptable salts.

Examples of preferred compounds of the formulas I I.5.1a, I.5.1b,I.6.1a, I.6.1b are 50

51

52

53

54

55

56

57

58

59

60

61

62

63

64

65

66

67

68

69

70

The present invention is also related to a pharmaceutical compositioncomprising at least one compound selected from the formulas Ia, Ib asdefined hereinbefore and at least one pharmaceutically acceptablecarrier or diluent. For this purpose, such a compound may be formulated,optionally together with other active substances as describedhereinafter, together with one or more inert conventional carriersand/or diluents, e.g. with corn starch, lactose, glucose,microcrystalline cellulose, magnesium stearate, polyvinylpyrrolidone,citric acid, tartaric acid, water, water/ethanol, water/glycerol,water/sorbitol, water/polyethylene glycol, propylene glycol,cetylstearyl alcohol, carboxymethylcellulose or fatty substances such ashard fat or suitable mixtures thereof, to produce conventional galenicpreparations such as plain or coated tablets, capsules, powders,granules, solutions, emulsions, syrups, aerosols for inhalation,ointments or suppositories.

Some expressions used hereinbefore and below to describe the compoundsaccording to the invention will now be defined more fully.

The term halogen denotes an atom selected from among F, Cl, Br and I,particularly F, Cl and Br.

The term C_(1-n)-alkyl, where n has a value of 3 to 8, denotes asaturated, branched or unbranched hydrocarbon group with 1 to n C atoms.Examples of such groups include methyl, ethyl, n-propyl, iso-propyl,butyl, iso-butyl, sec-butyl, tert-butyl.

A ring structure which is depicted as

with m being 0, 1 or 2 indicates a cyclopentyl (m=0), a cyclohexyl (m=1)or a cycloheptyl (m=2) ring.

As used herein, the designation whereby a bond to a substituent, forexample L, is drawn as emanating from the center of a ring, such as forexample,

means that the ring is i-times substituted with the same or differentsubstituents L which are attached to any free position on the ring thatwould otherwise be substituted by a hydrogen atom, unless specifiedotherwise.

The compounds according to this invention which are selected from thegroup of formulas Ia and Ib are made by methods well known to thoseskilled in the art from starting compounds known to those skilled in theart. The process chemistry is well known to those skilled in the art.Suitable reaction schemes and methods of synthesis are described forexample in Lazer et al., J. Med. Chem. 1997, 40, 980-989 and inLombardino et al., J. Med. Chem. 1971, 14, 973-977. Further synthesismethods of 3,4-dihydro-2H-1,2-benzothiazine 1,1-dioxide derivatives aredescribed by Suh et al. in the U.S. Pat. No. 4,683,306 and by Lombardinoin the U.S. Pat. No. 3,891,637.

An advantageous synthesis of the compounds according to this inventionis described by the following reaction schemes.

In the first step of the reaction scheme 1 a methyl substituted aromaticcompound of the formula A wherein the substituents are defined ashereinbefore is sulfonylated to yield a compound B or the correspondingsulfonyl acid derivative. With respect to the synthesis of compounds ofthe formulas I.3a, I.3b, I.4a, I.4b the corresponding starting materialsare for example methylated 1,2,3,4-tetrahydronaphthalene or indanecompounds. The sulfonylation is performed advantageously using ClSO₃H ora mixture of ClSO₃H and SO₂Cl₂. Preferred reaction temperatures are inthe range of −20° C. to +40° C., whereby the reaction is preferablystarted at lower temperatures and then continued at higher temperaturesof the given temperature range. The reaction may be carried out withoutsolvents or preferably with suitable aprotic solvents, more preferablyhalogenated hydrocarbons, as for example CH₃Cl, CH₂Cl₂ or CHCl₃.

The sulfonyl derivate of the formula B is treated with an amine NHR⁵,wherein R⁵ is defined as hereinbefore, to yield the sulfonamide derivateof the formula C. Preferred reaction temperatures are in the range of−20° C. to +40° C., whereby the reaction is preferably started at lowertemperatures and then continued at higher temperatures of the giventemperature range. Preferred solvents are ethers or alcohols, as forexample tetrahydrofuran, methanol, ethanol or propanol.

The sulfonamide derivative C is carboxylated at the methyl substituent.An advantageous carboxylation method employs butyllithium (BuLi) andcarbondioxide. The resulting carboxy-compound D is cyclodehydrated togive a dihydro-thiazine-3-one-1,1-dioxide of the formula E. Upontreatment with an optionally substituted phenyl isocyanate of theformula F1, in dimethylsulfoxide (DMSO) in the presence oftriethylamine, the compound E is converted to the final product of theformula G1. This reaction is preferably carried out in a temperaturerange between 10° C. and 50° C. Instead of the tertiary amine basesodium hydride (NaH) may be used whereby thedihydro-thiazine-3-one-1,1-dioxide of the formula E is reacted with NaHin tetrahydrofuran and then the optionally substituted phenyl isocyanateof the formula F1 is added to yield the final product of the formula G1.Suitable reaction temperatures are in the range of −20° C. and +40° C.

Alternatively, according to the reaction scheme 1b the intermediateproduct of the formual E is reacted with an isocyanate compound of theformula F2 in the presence of triethylamine or the intermediate productof the formula E is reacted with sodium hydride and afterwards with aisocyanate compound of the formula F2 to yield the amide of the formulaG2. In the above formula F2 X represents an optionally substituted alkylor aryl residue, for example n-butyl. Preferred reaction conditions aregiven in the description of the reaction scheme 1a.

In order to insert the desired anilide, the amide of the formula G2 isfirst converted to the corresponding ethyl ester H via ethanolysis, forexample, by refluxing in ethanol. The reaction of the ester H with thedesired anilide of the formula I yields the product of the formula J.Advantageous reaction conditions, including solvents of the abovedescribed steps from the carboxylation to the final reaction with theanilide are described in the literature, for example by Lombardino etal., J. Med. Chem. 1971, 14, 973-977.

Further synthesis methods of the compounds according to this inventionare described in the experimental section.

The method of the present invention relates to the treatment orprevention of a disease or condition in a mammal characterized by anincreased level of one or more amyloid β peptide isoforms, e.g., assoluble peptides as well as in the form of beta-amyloid plaques, inparticular by a pathological form of amyloid β peptide or fibrillar Aβisoforms, such as Aβ₄₂, and therefore the present invention allows forhelping to prevent or delay the onset of such a disease or condition.

Furthermore the method of the present invention relates to the treatmentor prevention of a disease or condition in a mammal characterized by achanged ratio of levels of Aβ isoforms, in particular by a changed ratioof a level of Aβ₄₀ to Aβ₄₂, and therefore the present invention allowsfor helping to prevent or delay the onset of such a disease orcondition. The term “changed ratio” means that the ratio of anindividual who is diagnosed to have the disease or condition ismeasurably different from the ratio of an individual who is diagnosednot to have the disease or condition. For example in patients diagnosedwith sporadic Alzheimer disease the ratio of a level of Aβ₄₀ to Aβ₄₂ isdecreased, i.e. the level of the Aβ₄₂ isoform is more elevated than thelevel of the Aβ₄₀ isoform, compared with an individual not affected byAlzheimers disease. As a further example, in a human not affected byAlzheimer's disease the ratio of the Aβ₄₀-level to the Aβ₄₂-level isabout 10 to 1 whereas in an individual affected by AD, in particular ADcaused by PS1 mutation, the ratio is shifted to about 3 to 1 or even 1to 1 or even lower.

For example, the methods and therefore the compounds of the inventionare useful for treating Alzheimer's disease, for helping to prevent ordelay the onset of Alzheimer's disease, for treating patients with MCI(mild cognitive impairment) and preventing or delaying the onset ofAlzheimer's disease in those who would progress from MCI to AD, fortreating Down's syndrome, for treating humans who have HereditaryCerebral Hemorrhage with Amyloidosis of the Dutch-Type, for treatingcerebral amyloid angiopathy and preventing its potential consequences,i.e., single and recurrent lobar hemorrhages, for treating otherdegenerative dementias, including dementias of mixed vascular anddegenerative origin, dementia associated with Parkinson's disease,dementia associated with progressive supranuclear palsy, dementiaassociated with cortical basal degeneration, and diffuse Lewy body typeAlzheimer's disease. The methods, compounds and compositions of theinvention are particularly useful for treating or preventing Alzheimer'sdisease. When treating or preventing these diseases, the compounds ofthe invention can either be used individually or in combination, as isbest for the patient.

As used herein, the term “treatment” means that the compounds of theinvention can be used in humans with at least a tentative diagnosis ofdisease. The compounds of the invention will delay, slow, or reverse theprogression of the disease thereby giving the individual a more usefullife span.

The term “prevention” means that the compounds of the present inventionare useful when administered to a patient who has not been diagnosed aspossibly having the disease at the time of administration, but who wouldnormally be expected to develop the disease or be at increased risk forthe disease. The compounds of the invention will slow the development ofdisease symptoms, delay the onset of the disease, or prevent theindividual from developing the disease at all.

Prevention also includes administration of the compounds of theinvention to those individuals thought to be predisposed to the diseasedue to age, familial history, genetic or chromosomal abnormalities,and/or due to the presence of one or more biological markers for thedisease, such as a known genetic mutation of APP or APP cleavageproducts in brain tissues or fluids.

The compounds of the invention are administered in a therapeuticallyeffective amount. The therapeutically effective amount will varydepending on the particular compound used and the route ofadministration, as is known to those skilled in the art.

The compounds of the invention can be administered orally, parenterally,(IV, IM, depo-IM, SQ, and depo SQ), sublingually, intranasally,inhalative, intrathecally, topically, or rectally. Dosage forms known tothose of skill in the art are suitable for delivery of the compounds ofthe invention.

Compositions are provided that contain therapeutically effective amountsof the compounds of the invention. The compounds are preferablyformulated into suitable pharmaceutical preparations such as tablets,capsules, or elixirs for oral administration or in sterile solutions orsuspensions for parenteral administration or aerosols for inhalativeadministration. Typically the compounds described above are formulatedinto pharmaceutical compositions using techniques and procedures wellknown in the art.

About 1 to 2000 mg, in particular 1 to 500 mg of a compound or mixtureof compounds of the invention or a physiologically acceptable saltthereof is admixed with a physiologically acceptable vehicle, carrier,excipient, binder, preservative, stabilizer, flavor, etc., in a unitdosage form as called for by accepted pharmaceutical practice. Theamount of active substance in those compositions or preparations is suchthat a suitable dosage in the range indicated is obtained. Thecompositions are preferably formulated in a unit dosage form, eachdosage containing from about 1 to about 1000 mg, more preferably about 1to about 200 mg of the active ingredient. The term “unit dosage form”refers to physically discrete units suitable as unitary dosages forhuman subjects and other mammals, each unit containing a predeterminedquantity of active material calculated to produce the desiredtherapeutic effect, in association with a suitable pharmaceuticalexcipient.

Pharmaceutical acceptable carriers or diluents suitable foradministration of the compounds provided herein include any suchcarriers or diluents known to those skilled in the art to be suitablefor the particular mode of administration. In addition, the activematerials can also be mixed with other active materials that do notimpair the desired action, or with materials that supplement the desiredaction, or have another action.

Pharmaceutically acceptable refers to those properties and/or substanceswhich are acceptable to the patient from a pharmacological/toxicologicalpoint of view and to the manufacturing pharmaceutical chemist from aphysical/chemical point of view regarding composition, formulation,stability, patient acceptance, and bioavailability.

The compounds may be formulated as the sole pharmaceutically activeingredient in the composition or may be combined with one or moredifferent active ingredients.

The concentration of the compound is effective for delivery of an amountupon administration that lessens or ameliorates at least one symptom ofthe disorder for which the compound is administered. Typically, thecompositions are formulated for single dosage administration.

The compounds and compositions of the invention can be enclosed inmultiple or single dose containers. The compounds and compositionsaccording to the invention can be provided in kits, for example,including component parts that can be assembled for use. For example, acompound according to this invention in lyophilized form and a suitablediluent may be provided as separated components for combination prior touse. A kit may include a compound according to this invention and asecond therapeutic agent for co-administration. The compound and secondtherapeutic agent may be provided as separate component parts. A kit mayinclude a plurality of containers, each container holding one or moreunit dose of the compound of the invention. The containers arepreferably adapted for the desired mode of administration, including,but not limited to tablets, gel capsules, sustained-release capsules,and the like for oral administration; depot products, pre-filledsyringes, ampules, vials and the like for parenteral administration; andpatches, medipads, creams, and the like for topical administration, andoptionally pre-filled inhalators for inhalative administration.

The concentration of active compound in the drug composition will dependon absorption, inactivation, and excretion rates of the active compound,the dosage schedule, and amount administered as well as other factorsknown to those of skill in the art.

It is to be further understood that for any particular subject, specificdosage regimens should be adjusted over time according to the individualneed and the professional judgment of the person administering orsupervising the administration of the compositions, and that theconcentration ranges set forth herein are exemplary only and are notintended to limit the scope or practice of the claimed method andcomposition.

Oral compositions will generally include an inert diluent or an ediblecarrier and may be compressed into tablets or enclosed in capsules. Forthe purpose of oral therapeutic administration, the active compound orcompounds can be incorporated with excipients and used in the form oftablets, capsules, lozenges, or troches.

Pharmaceutically compatible binding agents and adjuvant materials can beincluded as part of the composition.

The tablets, pills, capsules, troches, and the like can contain any ofthe following ingredients or compounds of a similar nature: a bindersuch as, but not limited to, gum tragacanth, acacia, corn starch, orgelatin; an excipient such as microcrystalline cellulose, starch, orlactose; a disintegrating agent such as, but not limited to, alginicacid and corn starch; a lubricant such as, but not limited to, magnesiumstearate; a glidant, such as, but not limited to, colloidal silicondioxide; a sweetening agent such as sucrose or saccharin; and aflavoring agent such as peppermint, methyl salicylate, or fruitflavoring.

When the dosage unit form is a capsule, it can contain, in addition tomaterial of the above type, a liquid carrier such as a fatty oil. Inaddition, dosage unit forms can contain various other materials, whichmodify the physical form of the dosage unit, for example, coatings ofsugar and other enteric agents. The compounds can also be administeredas a component of an elixir, suspension, syrup, wafer, chewing gum orthe like. A syrup may contain, in addition to the active compounds,sucrose as a sweetening agent and certain preservatives, dyes andcolorings, and flavors.

The active materials can also be mixed with other active materials thatdo not impair the desired action, or with materials that supplement thedesired action.

Methods for preparation of such formulations are known to those skilledin the art.

The oral dosage forms are administered to the patient 1, 2, 3, or 4times daily. It is preferred that the compounds of the invention beadministered either three or fewer times, more preferably once or twicedaily. Hence, it is preferred that the compounds of the invention beadministered in oral dosage form.

An administered amount therapeutically effective, especially whenadministered orally,

-   -   to modulate gamma-secretase activity, in particular such as to        lower the level of Aβ₄₂ or to increase the ratio of the        Aβ₄₀-level to the Aβ₄₂-level;    -   to inhibit A beta production, in particular to inhibit        Aβ₄₂-production;    -   to inhibit A beta deposition, in particular deposition of        fibrillar Aβ isoforms, e.g. of Aβ₄₂; or    -   to treat or prevent a neurodegenerative disorder, in particular        AD        is preferably from about 0.1 mg/day to about 2000 mg/day, more        preferably 0.1 mg/day to about 200 mg/day, in particular 0.5        mg/day to about 50 mg/day. It is understood that while a patient        may be started at one dose, that dose may be varied over time as        the patient's condition changes.

Given a particular compound of the invention and a desired dosage form,one skilled in the art would know how to prepare and administer theappropriate dosage form.

It should be apparent to one skilled in the art that the exact dosageand frequency of administration will depend on the particular compoundsof the invention administered, the particular condition being treated,the severity of the condition being treated, the age, weight, generalphysical condition of the particular patient, and other medication theindividual may be taking as is well known to administering physicianswho are skilled in this art.

Without being bound to any theory, there are indications suggesting thatthe compounds of the invention are suitable to modulate cleavage of APPat the gamma (γ) secretase cleavage site, or a mutant thereof, or at acorresponding site of a different isoform, such as APP751 or APP770, ora mutant thereof (sometimes (referred to as the “gamma secretase site”).While not wishing to be bound to a particular theory, modulation ofγ-secretase activity is thought to inhibit the production of toxic betaamyloid peptide (Aβ beta). Inhibitory activity is demonstrated in one ofa variety of inhibition assays, whereby cleavage of an APP substrate inthe presence of a γ-secretase enzyme is analyzed in the presence of theinhibitory compound, under conditions normally sufficient to result incleavage at the γ-secretase cleavage site. Reduction of APP cleavage atthe γ-secretase cleavage site compared with an untreated or inactivecontrol is correlated with inhibitory activity. Assay systems that canbe used to demonstrate efficacy of the compounds of the invention areknown, for example Aβ specific ELISA to quantify Aβ-levels are describedby Eriksen et al., 2003 and Weggen et al., 2001.

The enzymatic activity of γ-secretase and the production of A beta canbe analyzed in vitro or in vivo, using natural, mutated, and/orsynthetic APP substrates, natural, mutated, and/or recombinant enzyme,and the test compound. The analysis may involve primary or secondarycells expressing native, mutant, and/or recombinant APP and enzyme,animal models expressing native or mutated APP and enzyme, or mayutilize transgenic and non-transgenic animal models expressing thesubstrate and enzyme. Detection of enzymatic activity can be done byanalysis of one or more of the cleavage products, for example, by an invitro assay, in particular an Aβ secretion assay, fluorometric orchromogenic assay, HPLC, or other means of detection. Inhibitorycompounds are determined as those having the ability to decrease theamount of gamma-secretase cleavage product produced in comparison to acontrol, where gamma-secretase mediated cleavage in the reaction systemis observed and measured in the absence of inhibitory compounds.

Preferably the assay is carried out as follows:

Cell culture and drug treatment: U373 astrocytoma cells expressing humanwtAPP695 were used for screening compounds. Cells were cultured in 96well plates in DMEM medium, additionally supplemented with 10% FCS and1% glutamine, until they have grown to a confluent cell layer. The cellswere then incubated for 17 hours in the presence of the variousNSAID-analogues in DMEM medium. Afterwards, 100 μl of the supernatanthad been removed and measured with the ELISA as described below todetermine the Aβ₄₂ peptide concentrations. The cells were washed,incubated again for 4 hours with the compound, before measuring the Aβ₄₀levels. AlamarBlue assays (Serotec, Oxford, United Kingdom) wereconducted to determine cytotoxicity.

Sandwich ELISA for Aβ:

Monoclonal 6E10 against Aβ₁₋₁₇ (Signet Laboratories, Inc., Dedham,Mass., USA) was used to capture Aβ₄₀; SGY 3160 against Aβ₁₋₁₆ (MayoMedical Ventures, Rochester, Minn., USA) to capture Aβ₄₂. Bothantibodies were diluted in PBS at a concentration of 8 μg/ml to coat a96 well plate. Blocking was completed with 1% Block ACE (blockingreagent) (Dainippon Seiyaku, Asaka, Japan) in PBS for 2 hrs. The plateswere then washed with PBST and the cell supernatants, diluted 1:1.5 inEC buffer (0.1 M NaH₂PO₄, 0.1 M Na₂HPO₄, 2 mM EDTA, 0.4 M NaCl, 0.2%BSA, 0.05% CHAPS, 0.4% Block ACE, 0.05% NaN₃ pH 7.0) have been addedinto the wells, before the plates were stored at 4° C. over night.Detector antibodies (alkaline phosphatase-coupled ROβ40 and ROβ42against Aβ₄₀ and Aβ₄₂, respectively) were loaded onto the wells at 0.1μg/ml in ACE Block for 2 hrs. The reporter system used was the TropixELISA-Light chemiluminescent detection system (Applied Biosystems(Tropix), Bedford, Mass., USA).

In addition mass spectrometric methods can be employed for thedetermination of levels of isoforms of Aβ (see e.g. Eriksen et al.,2003; Weggen et al., 2003; Weggen et al., 2001).

Various animal models can be used to analyze gamma-secretase activityand/or processing of APP to release A beta, as described above. Forexample, transgenic animals overexpressing APP substrate can be used todemonstrate inhibitory activity of the compounds of the invention.Certain transgenic animal models have been described, for example, inU.S. Pat. Nos. 5,877,399; 5,612,486; 5,387,742; 5,720,936; 5,850,003;5,877,015 and 5,811,633, and in Games et. al., 1995, Nature 373: 523.Preferred are animals that exhibit characteristics associated with thepathophysiology of AD. Administration of the compound inhibitors of theinvention to the transgenic mice described herein provides analternative method for demonstrating the inhibitory activity of thecompounds. Administration of the compounds in a pharmaceuticallyeffective carrier and via an administrative route that reaches thetarget tissue in an appropriate therapeutic amount is also preferred.

Unless defined otherwise, all scientific and technical terms used hereinhave the same meaning as commonly understood by one of skill in the artto which this invention belongs. All patents and publications referredto herein are hereby incorporated by reference for all purposes. Thedefinitions and explanations below are for the terms as used throughoutthis entire document including both the specification and the claims.

Without further elaboration, it is believed that one skilled in the artcan, using the preceding description, practice the present invention toits fullest extent.

The following detailed examples describe how to prepare the variouscompounds and/or perform the various processes of the invention and areto be construed as merely illustrative, and not limitations of thepreceding disclosure in any way whatsoever. Those skilled in the artwill promptly recognize appropriate variations from the procedures bothas to reactants and as to reaction conditions and techniques.

All temperatures are in degrees Celsius.

EXAMPLE 13,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-carboxanilide1,1-dioxide

A solution of 5 g (19 mmol)3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide in 100 mL tetrahydrofuran was added to a suspension of 0.7 g(29 mmol) sodium hydride in 50 mL tetrahydrofuran at −5° C. under N₂.After termination of the hydrogen formation 5.7 g (48 mmol)phenylisocyanate dissolved in 50 mL tetrahydrofuran were added at −5° C.After stirring at room temperature (approx. 20° C.) the resultingmixture was quenched with ice/water and by addition of dilute HCl andthen extracted with CH₂Cl₂ (2 times). The combined CH₂Cl₂ extracts werewashed, dried and concentrated to give 6 g crude product. This materialwas recrystallized from ethanol to give 3.6 g3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-carboxanilide1,1-dioxide.

Yield: 54%

Melting point: 203-204° C.

Structure was confirmed by elementary analysis (C₂₀H₂₀N₂O₄S: C,H,N,S)and IR- and NMR-spectroscopy.

Preparation of the Starting Material:

To a solution of 124 g (0.84 mol)2-methyl-5,6,7,8-tetrahydro-naphthalene in 600 mL CHCl₃ 294 g (2.52 mol)chlorosulfonic acid at 0° C. were added. After 2 hrs at room temperaturethe solution was slowly poured onto ice. The organic phase was washed,dried and concentrated to give 231.4 g2-methyl-5,6,7,8-tetrahydro-naphthalene-2-sulfonic acid chloride useddirectly for the subsequent reaction.

231.4 g (0.84 mol) of the above sulfonic acid chloride were added to asolution of 57.5 g (1.8 mol) methylamine in 1.2 L ethanol at +5° C.followed by 192 g (1.9 mol) triethylamine. The mixture was stirred at+5° C. for 2 hrs and allowed to come to room temperature over 2 hrs. Thereaction mixture was concentrated and the residue taken up in ether,washed, dried, and concentrated. Recrystallization of the residue fromcyclohexane gave 136.1 g2-methyl-5,6,7,8-tetrahydro-naphthalene-3-sulfonic acid methylamide.

100 mL of a 1.5 molare (150 mmol) butyl lithium in hexane were added toa solution of 18 g (75 mmol)2-methyl-5,6,7,8-tetrahydro-naphthalene-3-sulfonic acid methylamide in200 mL tetrahydrofuran at −20° C. The resulting mixture was allowed tocome to room temperature and was poured onto a mixture of ether andsolid CO₂. After addition of water the resulting mixture was acidifiedwith dilute HCl and then extracted with CH₂Cl₂. The CH₂Cl₂ solution waswashed, dried and concentrated. Recrystallization from ether/petroleumether gave 15.8 g3-(N-methyl-sulfamoyl)-5,6,7,8-tetrahydro-naphthalene-2-acetic acid(melting point: 153-155° C.).

This naphthalene-2-acetic acid (14.7 g, 52 mmol) was refluxed 12 hrs in250 mL xylene with the addition of 0.2 g p-toluene-sulfonic acid. Thereaction mixture was cooled, filtered, washed with water andconcentrated. 13.5 g crude product were yielded.

EXAMPLE 23,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-methyl)carboxanilide1,1-dioxide

A solution of 2 g (7,5 mmol)3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide in 100 mL tetrahydrofuran was added to a suspension of 0.27g (11.3 mmol) sodium hydride in 50 mL tetrahydrofuran was added at −5°C. under N₂. After termination of the hydrogen formation 2.5 g (18.8mmol) p-methyl-phenylisocyanate dissolved in 50 mL tetrahdrofuran wereadded at −5° C. After stirring at room temperature the resulting mixturewas quenched with ice/water and by addition of dilute HCl and thenextracted with CH₂Cl₂ (2 times). The combined CH₂Cl₂ extracts werewashed, dried and concentrated to give the crude product. This materialwas recrystallized from ethanol to give 1.6 g3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-methyl)carboxanilide1,1-dioxide.

Yield: 54%

Melting point: 207-209° C.

Structure was confirmed by elementary analysis (C₂₁H₂₂N₂O₄S: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 33,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-fluor)carboxanilide1,1-dioxide

0.76 g (7.5 mmol) triethylamin were added to a solution of 2 g (7.5mmol)3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 1.03 g (7.5 mmol) p-fluor-phenylisocyanate dissolved in50 mL DMSO (dimethyl sulfoxide) at room temperature. After stirring for1 hr the resulting mixture was quenched with dilute HCl in an ice bathand then extracted with ether (2 times). The combined ether extractswere washed, dried and concentrated to give 2.3 g crude product. Thismaterial was recrystallized from ethanol to give 1.7 g3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-fluor)carboxanilide1,1-dioxide.

Yield: 56%

Melting point: 202-203° C.

Structure was confirmed by elementary analysis (C₂₀H₁₉FN₂O₄S: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 43,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-chloro)carboxanilide1,1-dioxide

Prepared from3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and p-chloro-phenylisocyanate analogous to example 1 andrecrystallized from ethanol.

Yield: 56%

Melting point: 203-205° C.

Structure was confirmed by elementary analysis (C₂₀H₁₉ClN₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

EXAMPLE 53,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(2,5-dichloro)carboxanilide1,1-dioxide

Prepared from3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 2,5-dichloro-phenylisocyanate analogous to example 3 andrecrystallization from ethylacetate

Yield: 59%

Melting point: 178-180° C.

Structure was confirmed by elementary analysis (C₂₀H₁₈Cl₂N₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

EXAMPLE 63,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(3,4-dichloro)carboxanilide1,1-dioxide

Prepared from3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 3,4-dichloro-phenylisocyanate analogous to example 1 andrecrystallization from ethylacetate.

Yield: 38%

Melting point: 226-228° C.

Structure was confirmed by elementary analysis (C₂₀H₁₈Cl₂N₂O₄S: C,H,N,S)and UV-, IR-, and NMR-spectroscopy.

EXAMPLE 73,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(3-chloro-4-methyl)carboxanilide1,1-dioxide

Prepared from3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 3-chloro-4-methyl-phenylisocyanate analogous to example3 and recrystallization from ethanol.

Yield: 76%

Melting point: 207-209° C.

Structure was confirmed by elementary analysis (C₂₁H₂₁ClN₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

EXAMPLE 83,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-bromo)carboxanilide1,1-dioxide

Prepared from3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 4-bromo-phenylisocyanate analogous to example 1 andrecrystallization from ethanol.

Yield: 33%

Melting point: 198-200° C.

Structure was confirmed by elementary analysis (C₂₀H₁₉BrN₂O₄S: C,H,N,S)and UV- and IR-spectroscopy.

EXAMPLE 93,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(2-chloro)carboxanilide1,1-dioxide

Prepared from3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 2-chloro-phenylisocyanate analogous to example 3 andrecrystallization from ethanol.

Yield: 42%

Melting point: 172-173° C.

Structure was confirmed by elementary analysis (C₂₀H₁₉ClN₂O₄S: C,H,N,S).

EXAMPLE 103,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(3-chloro)carboxanilide1,1-dioxide

Prepared from3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 2-chloro-phenylisocyanate analogous to example 3 andrecrystallization from ethanol.

Yield: 57%

Melting point: 182-184° C.

Structure was confirmed by elementary analysis (C₂₀H₁₉ClN₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

EXAMPLE 113,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-nitro)carboxanilide1,1-dioxide

Prepared from3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 4-nitro-phenylisocyanate analogous to example 1 andrecrystallization from ethanol.

Yield: 68%

Melting point: 205-207° C.

Structure was confirmed by elementary analysis (C₂₀H₁₉N₃O₆S: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 123,4,6,7,8,9-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-chloro)carboxanilide1,1-dioxide

Example 12 describes an alternative synthesis method compared to example4.

A mixture of3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-carboxylicacid ethylester 1,1-dioxide and 4-chloro-aniline in 75 mL toluene wasrefluxed under N₂ for 2 hrs. Ethanol was collected in a Dean-Stark trap.The remaining toluene was removed from the solution on a rotaryevaporator. The residue was treated with methylenechloride andrecrystallized from ethanol.

Yield: 87%

Melting point: 203-205° C.

Structure was confirmed by elementary analysis (C₂₀H₁₉ClN₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

Preparation of the Starting Material:

0.76 g (7.5 mmol) triethylamin were added to a solution of 2 g (7.5mmol)3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 0.765 g (7.5 mmol) n-butyl-isocyanate dissolved in 50 mLDMSO at room temperature. After stirring for 1 hr the resulting mixturewas quenched with dilute HCl in an ice bath and then extracted withether (2 times). The combined ether extracts were washed, dried andconcentrated to give 2.3 g crude product. This material wasrecrystallized from ethanol to give 2.1 g3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(n-butyl)carboxamide1,1-dioxide.

A solution of 2.1 g (6.0 mmol)3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(n-butyl)carboxamide1,1-dioxide in 100 mL ethanol was refluxed overnight under N₂. Solventwas removed on a rotary evaporator, the residue dissolved in ether.After washing, drying and concentrating the crude product was trituratedwith petroleum ether/methylenechloride to give 2.0 g3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-carboxylicacid ethylester 1,1-dioxide.

EXAMPLE 133,4,7,8,9,10-Hexahydro-2-methyl-3-oxo-2H-naphtho[2,1-e]-1,2-thiazine-4-(4-chloro)carboxanilide1,1-dioxide

A solution of 500 mg (1.9 mmol)3,4,7,8,9,10-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide in 100 mL tetrahydrofuran was added to a suspension of 68 mg(2.8 mmol) sodium hydride in 10 mL tetrahydrofuran at −5° C. under N₂.After termination of the hydrogen formation 720 mg (4.7 mmol)p-chlorophenylisocyanate dissolved in 5 mL tetrahydrofuran were added at−5° C. After stirring at room temperature the resulting mixture wasquenched with ice/water and by addition of dilute HCl and then extractedwith ether (2 times). The combined ether extracts were washed, dried andconcentrated to give crude product. This material was filtered on asilica gel column using CHCl₃ with 2% ethanol as eluant.Recrystallization of the eluated main fraction from cyclohexane/CHCl₃gave 300 mg3,4,7,8,9,10-hexahydro-2-methyl-3-oxo-2H-naphtho[2,1-e]-1,2-thiazine-4-(4-chloro)carboxanilide1,1-dioxide.

Yield: 38%

Melting point: 106-108° C.

Structure was confirmed by elementary analysis (C₂₀H₁₉ClN₂O₄S: C,H,N,S)and IR- and NMR-spectroscopy.

Preparation of the Starting Material:

A solution of 20 g (0.137 mol) 2-methyl-5,6,7,8-tetrahydro-naphthalenein 200 mL CHCl₃ was added to 48 g (0.412 mol) chlorosulfonic acid at 0°C. After 2 hrs at room temperature the solution was slowly poured ontoice. The organic phase was washed, dried and concentrated to give 32 g2-methyl-5,6,7,8-tetrahydro-naphthalene-sulfonic acid chloride useddirectly for the subsequent reaction.

32 g (0.137 mol) of the above sulfonic acid chloride were added to asolution of 10 g (0.3 mol) methylamine in 150 mL ethanol at +5° C. Themixture was stirred at +5° C. for 2 hrs and allowed to come to roomtemperature over 2 hrs. The reaction mixture was concentrated and theresidue taken up in ether, washed, dried, and concentrated. Afterseparation of the major reaction product (3-sulfonamide) bycrystallisation from cyclohexane the resulting solution was concentratedand filtered on silica gel using cyclohexane/ethylacetate (4:1) aseluant. Recrystallization of the major fraction gave 4.5 g2-methyl-5,6,7,8-tetrahydro-naphthaline-1-sulfonic acid methylamide.

18.3 mL of a 1.5 molare (40 mmol) butyl lithium in hexane were added toa solution of 4.5 g (19 mmol) sulfonic acid methylamide in 100 mLtetrahydrofuran at −20° C. The resulting mixture was allowed to come toroom temperature and was poured onto a mixture of ether and solid CO₂.After addition of water the resulting mixture acidified with dilute HCland the extracted with CH₂Cl₂. The CH₂Cl₂ solution was washed, dried andconcentrated: 3.8 g crude1-(N-methyl-sulfamoyl)-5,6,7,8-tetrahydro-naphthalene-2-acetic acid wasyielded.

This naphthalene-2-acetic acid (3.8 g) was refluxed 12 hrs in 250 mLxylene with the addition of 0.2 g p-toluene-sulfonic acid. The reactionmixture was cooled, filtered, washed with water and concentrated.Filtration on a silica gel column and recrystallization from cyclohexanegave 0.4 g3,4,7,8,9,10-hexahydro-2-methyl-3-oxo-2H-naphtho[2,1-e]-1,2-thiazine1,1-dioxide with a melting point: 90-92° C. The structure was confirmedby elementary analysis and IR-, UV- and NMR-spectroscopy.

EXAMPLE 146-Chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine-4-(2-trifluoromethyl)carboxanilide1,1-dioxide

At room temperature 77 mg (0.76 mmol) triethylamin were added to amixture of 250 mg (0.74 mmol)6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine1,1-dioxide and 142 mg (0.76 mmol) o-trifuoromethyl-phenylisocyanatedissolved in 3 mL DMSO. After stirring for 2.5 hrs the resulting mixturewas quenched with dilute HCl in an ice bath and then extracted withmethylenechloride (2 times). The combined extracts were washed, driedand concentrated to give 380 mg crude product. This material wasrecrystallized from methylenechloride/hexane to give 263 mg6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine-4-(2-trifluoromethyl)carboxanilide1,1-dioxide.

Yield: 68%

Melting point: 198-199° C.

Structure was confirmed by elementary analysis (C₂₃H₁₅F₄ClN₂O₄S: C,H,N)and mass-spectroscopy.

Preparation of the Starting Material:

25.0 g p-fluorobenzylamine and 15.9 ml triethylamine were added to asolution of 12.4 g (55.6 mmol) 4-chloro-2-methyl-phenylsulfonic acidchloride in 150 ml tetrahydrofuran at 5° C. The mixture was stirred at+5° C. for 20 mins and 3.5 hrs at room temperature. The reaction mixturewas poured into water and extracted into methylenechloride, washed,dried, and concentrated to give 16.4 g crude material.

60 ml of a 2.5 molare butyl lithium solution in hexane were added to asolution of 16.4 (52.4 mmol)4-chloro-2-methyl-benzosulfon-(4-fluorobenzyl)amide in 225 mltetrahydrofuran at −5° C. The resulting mixture was allowed to come toroom temperature and was poured onto a mixture of ether and solid CO₂.After addition of water the resulting mixture acidified with dilute HCland then extracted with CH₂Cl₂. The CH₂Cl₂ solution was washed, driedand concentrated. Filtration on a silica gel column gave 11.1 g5-chloro-1-(N-4-fluorobenzyl-sulfamoyl)-phenyl-acetic acid. Thisphenyl-acetic acid (2.86 g, 8.8 mmol) was refluxed 12 hrs in 50 mLxylene with the addition of 5 mg p-toluene-sulfonic acid. The reactionmixture was cooled, filtered, washed with water and concentrated.Recrystallization from methylenechloride/hexane gave 1.63 g6-chloro-3,4-dihydro-2-(4-fluorbenzyl)-3-oxo-2H-1.2-benzothiazine1.1-dioxide. Melting point 132-133° C. Yield 55%.

EXAMPLE 156-Chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine-4-(3-trifluoromethyl)carboxanilide1,1-dioxide

At room temperature 70 mg (0.7 mmol) triethylamin were added to amixture of 250 mg (0.74 mmol)6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine1,1-dioxide and 130 mg (0.7 mmol) o-trifuoromethyl-phenylisocyanatedissolved in 3 mL DMSO. After stirring for 2.5 hrs the resulting mixturewas quenched with dilute HCl in an ice bath and then extracted withmethylenechloride (2 times). The combined extracts were washed, driedand concentrated to give 380 mg crude product. This material wasrecrystallized from methylenechloride/hexane to give 240 mg6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine-4-(3-trifluoromethyl)carboxanilide1,1-dioxide.

Yield: 62%

Melting point: 183-184° C.

Structure was confirmed by elementary analysis (C₂₃H₁₅F₄ClN₂O₄S: C,H,N)and mass-spectroscopy.

EXAMPLE 166-Chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine-4-(3,5-bis(trifluoromethyl))carboxanilide1,1-dioxide

At room temperature 76 mg (0.75 mmol) triethylamin were added to amixture of 250 mg (0.74 mmol)6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine1,1-dioxide and 192 mg (0.75 mmol)3,5-bis(trifluoromethyl)-phenylisocyanate dissolved in 3 mL DMSO. Afterstirring for 2.5 hrs the resulting mixture was quenched with dilute HClin an ice bath and then extracted with methylenechloride (2 times). Thecombined extracts were washed, dried and concentrated to give 390 mgcrude product. This material was recrystallized frommethylenechloride/hexane to give 303 mg6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine-4-(3-trifluoromethyl)carboxanilide1,1-dioxide.

Yield: 69%

Melting point: 233-234° C.

Structure was confirmed by elementary analysis (C₂₃H₁₄F₄ClN₂O₄S: C,H,N)and mass-spectroscopy.

EXAMPLE 176-Chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine-4-(2,4-dibromo)carboxanilide1,1-dioxide

A mixture of 550 mg (1.34 mmol)6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1.2-benzothiazine-4-carboxylicacid ethylester 1,1-dioxide and 351 mg 2,4-dibromoaniline in 50 mLtoluene was refluxed under N₂ for 2 hrs. Ethanol was collected in aDean-Stark trap. The remaining toluene was removed from the solution ona rotary evaporator. The residue was recrystallized frommethylenechloride/hexane to give 484 mg6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine-4-(2,4-dibromo)carboxanilide1,1-dioxide

Yield: 62%

Melting point: 222-223° C.

Structure was confirmed by elementary analysis (C₂₂H₁₇FCl Br₂N₂O₄S:C,H,N) and NMR- and mass-spectroscopy.

Preparation of the Starting Material:

At room temperature 77 mg (0.76 mmol) triethylamin were added to amixture of 250 mg (0.74 mmol)6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine1,1-dioxide and 75 mg (0.76 mmol) n-butylisocyanate dissolved in 3 mLDMSO. After stirring for 2.5 hrs the resulting mixture was quenched withdilute HCl in an ice bath and then extracted with methylenechloride (2times). The combined extracts were washed, dried and concentrated togive 310 mg crude product. This material was recrystallized frommethylenechloride/hexane to give 240 mg6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1,2-benzothiazine-4-(n-butyl)carboxamide1,1-dioxide.

A solution of 210 mg6-chloro-3,4-dihydro-2-(4-fluorbenzyl)-3-oxo-2H-1,2-benzothiazine-4-(n-butyl)carboxamide1,1-dioxide in 20 mL ethanol was refluxed overnight under N₂. Thesolvent was removed on a rotary evaporator, the residue dissolved inether. After washing, drying and concentrating the crude product wastriturated with petroleum ether/methylenechloride to give 200 mg6-chloro-3,4-dihydro-2-(4-fluorobenzyl)-3-oxo-2H-1.2-benzothiazine-4-carboxylicacid ethylester 1,1-dioxide.

EXAMPLE 183,4-Dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-carboxanilide1,1-dioxide

To a solution of 1.3 g (5 mmol)3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine 1,1-dioxideand 0.7 ml (5 mmol) triethylamin dissolved in 10 ml DMSO at roomtemperature was added 0.6 g (5 mmol) phenylisocyanate. After stirringfor 20 hr the resulting mixture was quenched with dilute HCl in an icebath and then extracted with ether (2 times). The combined etherextracts were washed, dried and concentrated to give 1.9 g crudeproduct. This material was recrystallized from ethanol followed byrecrystallization from ethylacetate to give 0.7 g3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-carboxanilide1,1-dioxide.

Yield: 37%

Melting point: 188-190° C.

Structure was confirmed by elementary analysis (C₂₀H₁₆N₂O₄S: C,H,N,S)and IR- and NMR-spectroscopy.

Preparation of the Starting Material:

To a solution of 124 g (0.84 mol)2-methyl-5,6,7,8-tetrahydro-naphthalene in 600 mL CHCl₃ 294 g (2.52 mol)chlorosulfonic acid at 0° C. were added. After 2 hrs at room temperaturethe solution was slowly poured onto ice. The organic phase was washed,dried and concentrated to give 231.4 g2-methyl-5,6,7,8-tetrahydro-naphthalene-2-sulfonic acid chloride useddirectly for the subsequent reaction. To a solution of 57.5 g (1.8 mol)methylamine in 1.2 L ethanol were added at +5° C. 231.4 g (0.84 mol) ofthe above sulfonic acid chloride followed by 192 g (1.9 mol)triethylamine. The mixture was stirred at +5° C. for 2 hrs and allowedto come to room temperature over 2 hrs. The reaction mixture wasconcentrated and the residue taken up in ether, washed, dried, andconcentrated. Recrystallization of the residue from cyclohexane gave136.1 g 2-methyl-5,6,7,8-tetrahydro-naphthalene-3-sulfonic acidmethylamide.

This compound was dehydrogenated by use of DDQ(2,3-dichloro-5,6-dicyano-benzoquinone) in 32% yield to2-methyl-naphthalene-(N-methyl)3-sulfonamide (melting point 139-140°C.).

To a solution of 4.5 g (19 mmol)2-methyl-naphthalene-3-(N-methyl)sulfonamide in 200 mL tetrahydrofuraneat −20° C. was added 100 mL of a 1.5 molare (40 mmol) butyl lithium inhexane. The resulting mixture was allowed to come to room temperatureand was poured onto a mixture of ether and solid CO₂. After addition ofwater the resulting mixture acidified with dilute HCl and the extractedwith CH₂Cl₂. The CH₂Cl₂ solution was washed, dried and concentrated.Recrystallization from ethylene chloride gave 2.6 g3-(N-methyl-sulfamoyl)-naphthalene-2-acetic acid (melting point:185-186° C.).

This naphthalene-2-acetic acid (2.6 g, 9.4 mmol) was 12 hrs refluxed in100 mL xylene with the addition of 0.2 g p-toluene-sulfonic acid. Thereaction mixture was cooled, filtered, washed with water andconcentrated. Recrystallization from ethanol gave 1.5 g (61%)3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine 1,1-dioxide(melting point: 126-127° C.).

EXAMPLE 193,4-Dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-methyl)carboxanilide 1,1-dioxide

To a suspension of 0.276 g (11.5 mmol) sodium hydride in 20 mLtetrahydrofurane was added at −5° C. under N₂ a solution of 2 g (7.6mmol) 3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide in 30 mL tetrahydrofurane. After termination of the hydrogenformation 2.56 g (19.2 mmol) p-methyl-phenylisocyanate dissolved in 50mL tetrahydrofurane were added at −5° C. After stirring at roomtemperature the resulting mixture was quenched with ice/water and byaddition of dilute HCl and then extracted with CH₂Cl₂ (2 times). Thecombined CH₂Cl₂ extracts were washed, dried and concentrated to give 6 gcrude product. This material was recrystallized from ethanol to give 2.1g3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-methyl)carboxanilide1,1-dioxide.

Yield: 83%

Melting point: 223-225° C.

Structure was confirmed by elementary analysis (C₂₁H₁₈N₂O₄S: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 203,4-Dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(3-fluoro)carboxanilide 1,1-dioxide

Prepared from 3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and m-fluoro-phenylisocyanate analogous to example 19 andrecrystallized from ethanol.

Yield: 46%

Melting point: 191-192° C.

Structure was confirmed by elementary analysis (C₂₀H₁₅FN₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

EXAMPLE 213,4-Dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-fluoro)carboxanilide 1,1-dioxide

Prepared from 3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and p-fluoro-phenylisocyanate analogous to example 19 andrecrystallized from ethanol.

Yield: 52%

Melting point: 235-237° C.

Structure was confirmed by elementary analysis (C₂₀H₁₅FN₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

EXAMPLE 223,4-Dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(2-chloro)carboxanilide 1,1-dioxide

Prepared from 3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and o-chloro-phenylisocyanate analogous to example 19 andrecrystallization from ethylacetate

Yield: 52%

Structure was confirmed by elementary analysis (C₂₀H₁₅ClN₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

EXAMPLE 233,4-Dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(2,5-dichloro)carboxanilide 1,1-dioxide

Prepared from3,4,6,7,8,9-hexahydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 2,5-dichloro-phenylisocyanate analogous to example 19and recrystallization from ethanol.

Yield: 63%

Structure was confirmed by elementary analysis (C₂₀H₁₈Cl₂N₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

EXAMPLE 243,4-Dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(3-chloro-4-methyl)carboxanilide 1,1-dioxide

Prepared from 3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 3-methyl-4-chloro-phenylisocyanate analogous to example19 and recrystallization from ethylacetate.

Yield: 65%

Structure was confirmed by elementary analysis (C₂₁H₁₇ClN₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

EXAMPLE 253,4-Dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-bromo)carboxanilide1,1-dioxide

Prepared from 3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 4-bromo-phenylisocyanate analogous to example 19 andrecrystallization from ethanol.

Yield: 76%

Structure was confirmed by elementary analysis (C₂₀H₁₅BrN₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

EXAMPLE 263,4-Dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(3-trifluoromethyl)carboxanilide 1,1-dioxide

Prepared from 3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 3-trifluoro-phenylisocyanate analogous to example 19 andrecrystallization from cyclohexane/ethylacetate.

Yield: 41%

Melting point: 148-150° C.

Structure was confirmed by elementary analysis (C₂₁H₁₅F₃N₂O₄S: C,H,N,S)and UV- and IR-spectroscopy.

EXAMPLE 273,4-Dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-nitro)carboxanilide1,1-dioxide

Prepared from 3,4-dihydro-2-methyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 4-nitro-phenylisocyanate analogous to example 19 andrecrystallization from ethanol.

Yield: 49%

Structure was confirmed by elementary analysis (C₂₀H₁₅N₃O₆S: C,H,N,S).

EXAMPLE 283,4-Dihydro-2-ethyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine-4-(4-chloro)carboxanilide1,1-dioxide

Prepared from 3,4-dihydro-2-ethyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide and 4-chloro-phenylisocyanate analogous to example 19 andrecrystallization from ethanol.

Yield: 57%

Melting point: 206-208° C.

Structure was confirmed by elementary analysis (C₂₁H₁₇ClN₂O₄S: C,H,N,S)and UV-, IR- and NMR-spectroscopy.

Preparation of the Starting Material:

A solution of 7 g (31.6 mmol) 3-methyl-naphthalene-2-sulphonamide 1.27 g(31.6 mmol) sodium hydroxide and 9.83 g (63 mmol) ethyliodine in 500 mlethanol was stirred for 72 hrs. The solvent was removed using anevaporator and the resulting residue was filtered on a silica gel columnusing methylenchloride and ethanol as solvent. Recrystallization fromcyclohexane/ethylacetate resulted in 3.5 g (45%)3-methyl-naphthalene-2-(N-ethyl)sulphonamide (melting point: 208-209°C.). 3.5 g (12 mmol) 2-methyl-naphthalene-3-(N-ethyl)sulfonamide weretransformed into 3-(N-ethyl-sulfamoyl)-naphthalene-2-acetic acid(melting point: 168-170° C.) as described in example 1.

This naphthalene-2-acetic acid (1.4 g, 4 mmol) was 12 hrs refluxed in250 mL xylene with the addition of 0.2 g p-toluene-sulfonic acid. Thereaction mixture was cooled, filtered, washed with water andconcentrated. Recrystallization from cyclohexane/ethylacetate to give1.1 g (83%) 3,4-dihydro-2-ethyl-3-oxo-2H-naphtho[2,3-e]-1,2-thiazine1,1-dioxide, melting point 170-171° C.

EXAMPLE 293,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-carboxanilide1,1-dioxide

To a suspension of 0.78 g (32.5 mmol) sodium hydride in 50 mLtetrahydrofurane was added at −5° C. under N₂ a solution of 5 g (21.6mmol) 3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine1,1-dioxide in 50 mL tetrahydrofurane. After termination of the hydrogenformation 6.5 g (55 mmol) phenylisocyanate dissolved in 50 mLtetrahydrofurane were added at −5° C. After stirring at room temperaturethe resulting mixture was quenched with ice/water and by addition ofdilute HCl and then extracted with CH₂Cl₂ (2 times). The combined CH₂Cl₂extracts were washed, dried and concentrated to give 6 g crude product.This material was recrystallized from ethanol to give 5.2 g3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine-4-carboxanilide1,1-dioxide.

Yield: 69%

Melting point: 182-184° C.

Structure was confirmed by elementary analysis (C₁₅H₁₄N₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

Preparation of the Starting Material:

2,5-dimethylthiophene was transformed to2,5-dimethyl-thiophene-3-(N-methyl)sulfonamide (melting point: 70-71°C.) analogous to example 19. Subsequent reaction with butyllithium andcarbon dioxide yielded 5-methyl-3-(N-methyl)aminosulfonyl-thiophene2-acetic acid (melting point: 109° C.) and cyclization with p-toluenesulfonic acid3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine1,1-dioxide.

Melting point: 119-120° C.

Structure was confirmed by elementary analysis (C₈H₉NO₃S₂: C,H,N,S) andIR- and NMR-spectroscopy.

EXAMPLE 303,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(4-methyl)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 4-methyl-phenylisocyanate analogous to example 29 andrecrystallization from ethanol.

Yield: 58%

Melting point: 200-201° C.

Structure was confirmed by elementary analysis (C₁₆H₁₆N₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 313,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(4-fluoro)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 4-fluoro-phenylisocyanate analogous to example 29 andrecrystallization from ethanol.

Yield: 56%

Melting point: 191-193° C.

Structure was confirmed by elementary analysis (C₁₅H₁₃FN₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 323,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(2,4-difluoro)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 2,4-difluoro-phenylisocyanate analogous to example 29 andrecrystallization from benzene/petroleum ether.

Yield: 72%

Melting point: 144-145° C.

Structure was confirmed by elementary analysis (C₁₅H₁₃F₂N₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 333,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(3,4-dichloro)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 2,4-dichloro-phenylisocyanate analogous to example 29 andrecrystallization from ethanol.

Yield: 19%

Melting point: 179-180° C.

Structure was confirmed by elementary analysis (C₁₅H₁₃Cl₂N₂O₄S₂:C,H,N,S).

EXAMPLE 343,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(3-chloro-4-methyl)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 3-chloro-4-methylphenylisocyanate analogous to example 29 andrecrystallization from isopropanol.

Yield: 42%

Melting point: 186-188° C.

Structure was confirmed by elementary analysis (C₁₆H₁₅ClN₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 353,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(4-bromo)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 4-bromophenylisocyanate analogous to example 29 andrecrystallization from benzene/petroleum ether.

Yield: 22%

Melting point: 138-140° C.

Structure was confirmed by elementary analysis (C₁₅H₁₃BrN₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 363,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(3-trifluoromethyl)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 3-trifluoromethylphenylisocyanate analogous to example 29 andrecrystallization from benzene/petroleum ether.

Yield: 50%

Melting point: 103-104° C.

Structure was confirmed by elementary analysis (C₁₆H₁₃F₃N₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 373,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(4-trifluoromethyl)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 4-trifluoromethylphenylisocyanate analogous to example 29 andrecrystallization from cyclohexane/chloroform.

Yield: 50%

Melting point: 103-104° C.

Structure was confirmed by elementary analysis (C₁₆H₁₃F₃N₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 383,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(4-methoxy)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 4-methoxyphenylisocyanate analogous to example 29 andrecrystallization from ethanol.

Yield: 61%

Melting point: 176-178° C.

Structure was confirmed by elementary analysis (C₁₆H₁₆N₂O₅S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 393,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(4-nitro)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 4-nitrophenylisocyanate analogous to example 29.

Yield: 52%

EXAMPLE 403,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(4-nitro)carboxanilide 1,1-dioxide Cyclohexylamine Salt

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine-4-(4-nitro)carboxanilide1,1-dioxide and cyclohexylamine and recrystallization fromwater/ethanol.

Yield: 95%

Melting point: 208-209° C.

Structure was confirmed by elementary analysis (C₂₁H₂₆N₄O₆S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 413,4-Dihydro-2,6-dimethyl-3-oxo-2H-furo[2,3-e]-1.2-thiazine-4-(4-methyl)carboxanilide 1,1-dioxide

To a suspension of 0.54 g (22 mmol) sodium hydride in 50 mLtetrahydrofurane was added at −5° C. under N₂ a solution of 4 g (18.6mmol) 3,4-dihydro-2,6-dimethyl-3-oxo-2H-furo[2,3-e]-1,2-thiazine1,1-dioxide in 50 mL tetrahydrofurane. After termination of the hydrogenformation 6.5 g (55 mmol) 4-methylphenylisocyanate dissolved in 50 mLtetrahydrofurane were added at −5° C. After stirring at room temperaturethe resulting mixture was quenched with ice/water and by addition ofdilute HCl and then extracted with CH₂Cl₂ (2 times). The combined CH₂Cl₂extracts were washed, dried and concentrated to give 5.7 g crudeproduct. This material was recrystallized from benzene to give 4 g3,4-dihydro-2,6-dimethyl-3-oxo-2H-furo[2,3-e]-1,2-thiazine-4-(4-methyl)carboxanilide1,1-dioxide.

Yield: 62%

Melting point: 210-212° C.

Structure was confirmed by elementary analysis (C₁₆H₁₆N₂O₅S: C,H,N,S)and IR- and NMR-spectroscopy.

Preparation of the Starting Material:

2,5-dimethylfurane was transformed to2,5-dimethyl-furane-3-(N-methyl)sulfonamide analogous to example 19.Subsequent reaction with n-butyllithium and carbon dioxide yielded5-methyl-3-(N-methyl)aminosulfonyl-furane 2-acetic acid (melting point:112-113° C.) and cyclization with phosphorous pentachloride3,4-dihydro-2,6-dimethyl-3-oxo-2H-furo[2,3-e]-1,2-thiazine 1,1-dioxide.

Melting point: 132-133° C.

Structure was confirmed by elementary analysis (C₈H₉NO₃S: C,H,N,S) andIR- and NMR-spectroscopy.

EXAMPLE 423,4-Dihydro-2,6-dimethyl-3-oxo-2H-furo[2,3-e]-1.2-thiazine-4-(4-bromo)carboxanilide 1,1-dioxide

Prepared from 3,4-dihydro-2,6-dimethyl-3-oxo-2H-furo[2,3-e]-1,2-thiazine1,1-dioxide and 4-bromophenylisocyanate analogous to example 41 andrecrystallization from cyclohexane.

Yield: 72%

Melting point: 180-181° C.

Structure was confirmed by elementary analysis (C₁₅H₁₃BrN₂O₅S: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 433,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1.2-thiazine-4-carboxanilide1,1-dioxide

To a suspension of 0.82 g (34 mmol) sodium hydride in 50 mLtetrahydrofurane was added at −5° C. under N₂ a solution of 5.3 g (23mmol) 3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1,2-thiazine1,1-dioxide in 50 mL tetrahydrofurane. After termination of the hydrogenformation 6.5 g (55 mmol) phenylisocyanate dissolved in 50 mLtetrahydrofurane were added at −5° C. After stirring at room temperaturethe resulting mixture was quenched with ice/water and by addition ofdilute HCl and then extracted with CH₂Cl₂ (2 times). The combined CH₂Cl₂extracts were washed, dried and concentrated to give 6 g crude product.This material was recrystallized from ethanol to give 4.8 g3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1,2-thiazine-4-carboxanilide1,1-dioxide.

Yield: 60%

Melting point: 184-185° C.

Structure was confirmed by elementary analysis (C₁₅H₁₄N₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

Preparation of the Starting Material:

2,4-dimethylthiophene was transformed to3,5-dimethyl-thiophene-2-(N-methyl)sulfonamide analogous to example 19.Subsequent reaction with butyllithium and carbon dioxide yielded5-methyl-2-(N-methyl)aminosulfonyl-thiophene 3-acetic acid (meltingpoint: 138° C.) and cyclization with p-toluene sulfonic acid3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1,2-thiazine1,1-dioxide.

Melting point: 83-84° C.

Structure was confirmed by elementary analysis (C₈H₉NO₃S₂: C,H,N,S) andIR- and NMR-spectroscopy.

EXAMPLE 443,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1.2-thiazine-4-(4-methyl)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1,2-thiazine 1,1-dioxideand 4-methyl-phenylisocyanate analogous to example 43 andrecrystallization from ethanol.

Yield: 60%

Melting point: 185° C.

Structure was confirmed by elementary analysis (C₁₆H₁₆N₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 453,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1.2-thiazine-4-(2-fluoro)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1,2-thiazine 1,1-dioxideand 2-fluoro-phenylisocyanate analogous to example 43 andrecrystallization from ethanol.

Yield: 95%

Melting point: 159-160° C.

Structure was confirmed by elementary analysis (C₁₅H₁₃FN₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 463,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1.2-thiazine-4-(4-fluoro)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1,2-thiazine 1,1-dioxideand 4-fluoro-phenylisocyanate analogous to example 43 andrecrystallization from ethanol.

Yield: 96%

Melting point: 173-174° C.

Structure was confirmed by elementary analysis (C₁₅H₁₃FN₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 473,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1.2-thiazine-4-(4-bromo)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1,2-thiazine 1,1-dioxideand 4-bromo-phenylisocyanate analogous to example 43 andrecrystallization from ethyl acetate.

Yield: 77%

Melting point: 180-182° C.

Structure was confirmed by elementary analysis (C₁₅H₁₃BrN₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 483,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1.2-thiazine-4-(3-trifluoromethyl)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1,2-thiazine 1,1-dioxideand 3-trifluoromethyl-phenylisocyanate analogous to example 43 andrecrystallization from isopropanol.

Yield: 65%

Melting point: 163-164° C.

Structure was confirmed by elementary analysis (C₁₆H₁₃F₃N₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 493,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1.2-thiazine-4-(4-trifluoromethyl)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1,2-thiazine 1,1-dioxideand 4-trifluoromethyl-phenylisocyanate analogous to example 43 andrecrystallization from ethanol.

Yield: 69%

Melting point: 190° C.

Structure was confirmed by elementary analysis (C₁₆H₁₃F₃N₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

EXAMPLE 503,4-Dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1.2-thiazine-4-(2-fluoro)carboxanilide 1,1-dioxide

Prepared from3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[2,3-e]-1,2-thiazine 1,1-dioxideand 2-fluorophenylisocyanate analogous to example 29 andrecrystallization from ethanol.

Yield: 64%

Melting point: 169-170° C.

Structure was confirmed by elementary analysis (C₁₅H₁₃FN₂O₄S₂: C,H,N,S)and IR- and NMR-spectroscopy.

Examples of Pharmaceutical Formulations A) Tablets per tablet activesubstance 50 mg lactose 170 mg corn starch 260 mg polyvinylpyrrolidone15 mg magnesium stearate 5 mg 500 mg

The finely ground active substance, lactose and some of the corn starchare mixed together. The mixture is screened, then moistened with asolution of polyvinylpyrrolidone in water, kneaded, wet-granulated anddried. The granules, the remaining corn starch and the magnesiumstearate are screened and mixed together. The mixture is compressed toproduce tablets of suitable shape and size. B) Tablets per tablet activesubstance 40 mg corn starch 210 mg lactose 65 mg microcrystallinecellulose 40 mg polyvinylpyrrolidone 20 mg sodium-carboxymethyl starch23 mg magnesium stearate 2 mg 400 mg

The finely ground active substance, some of the corn starch, lactose,microcrystalline cellulose and polyvinylpyrrolidone are mixed together,the mixture is screened and worked with the remaining corn starch andwater to form a granulate which is dried and screened. Thesodium-carboxymethyl starch and the magnesium stearate are added andmixed in and the mixture is compressed to form tablets of a suitablesize. 3C) Coated tablets per coated tablet Active substance 5 mg Cornstarch 41.5 mg Lactose 30 mg Polyvinylpyrrolidone 3 mg Magnesiumstearate 0.5 mg 80 mg

The active substance, corn starch, lactose and polyvinylpyrrolidone arethoroughly mixed and moistened with water. The moist mass is pushedthrough a screen with a 1 mm mesh size, dried at about 45° C. and thegranules are then passed through the same screen. After the magnesiumstearate has been mixed in, convex tablet cores with a diameter of 6 mmare compressed in a tablet-making machine. The tablet cores thusproduced are coated in known manner with a covering consistingessentially of sugar and talc. The finished coated tablets are polishedwith wax. D) Capsules per capsule Active substance 25 mg Corn starch283.5 mg Magnesium stearate 1.5 mg 310 mg

The substance and corn starch are mixed and moistened with water. Themoist mass is screened and dried. The dry granules are screened andmixed with magnesium stearate. The finished mixture is packed into size1 hard gelatine capsules. E) Ampoule solution active substance 0,5 mgsodium chloride 50 mg water for inj. 5 ml

The active substance is dissolved in water at its own pH or optionallyat pH 5.5 to 6.5 and sodium chloride is added to make it isotonic. Thesolution obtained is filtered free from pyrogens and the filtrate istransferred under aseptic conditions into ampoules which are thensterilised and sealed by fusion. The ampoules contain 0.5 mg, 2.5 mg and5.0 mg of active substance. F) Suppositories Active substance 30 mgSolid fat 1670 mg 1700 mg

The solid fat is melted. The ground active substance is homogenouslydispersed at 40° C. It is cooled to 38° C. and poured into slightlychilled suppository moulds.

1. A compound selected from the formulas IIa, IIb

wherein - - - - represents a single or a double bond, such that the ringcontaining the groups V and W is a phenyl, a furanyl or a thiophenylring; V is defined as —CR1═ or Q, and in case W is Q, then V is a singlebond; W is defined as ═CR4— or Q, and in case V is Q, then W is a singlebond; Q is O or S; Y is —(C═O)— or —(SO2)—; R1, R4 are eachindependently selected from the group consisting of H, F, Cl, Br, CN,CF3, C1-4-alkyl and C1-4-alkoxy; and R2, R3 are each independentlyselected from the group consisting of H, F, Cl, Br, CN, CF3, C1-4-alkyland C1-4-alkoxy; or in case V is —CR1═ and W is ═CR4—, the substituentsR2 and R3 may be linked together forming with the C-atoms to which theyare attached to a C5-7-cycloalkyl, C5-7-cycloalkenyl or a phenyl group,wherein a cycloalkyl, cycloalkenyl or phenyl ring may be substitutedwith one or more substituents L2; or in case V is —CR1═ and W is ═CR4—,the substituents R1 and R2 may be linked together forming with theC-atoms to which they are attached to a C5-7-cycloalkyl,C5-7-cycloalkenyl or a phenyl group, wherein a cycloalkyl, cycloalkenylor phenyl ring may be substituted with one or more substituents L2; R6is H or C1-4-alkyl; L1 is each independently selected from the groupconsisting of C1-4-alkyl, C1-3-alkoxy, F, Cl, Br, CN, NO2 and CF3; L2,L3 is each independently selected from the group consisting ofC1-4-alkyl, F, Cl, Br, CN and CF3; i is 0, 1, 2, 3, 4 or 5; k is 1, 2,3, 4 or 5; or a pharmaceutically acceptable salt thereof.
 2. A compoundaccording to claim 1 wherein the compound is selected from the formulaII.1a and II.1b

wherein the group Y, the substituents R1, R4, R6, L1 and L3 and theindex i and k are defined as in claim 36, and R2, R3 are eachindependently selected from the group consisting of H, F, Cl, Br, CN,CF3, C1-4-alkyl and C1-4-alkoxy; or or a pharmaceutically acceptablesalt thereof.
 3. A compound according to claim 1, selected from thegroup consisting of

or a pharmaceutically acceptable salt thereof.